FCC ID 2ASFG-SONOCHART

Dental ultrasonic probe

by Carestream Dental, LLC

Grantee Code: 2ASFG   Product Code: SONOCHART
Latest application date: 2024-08-08

FCC ID Device Details

FCC ID2ASFG-SONOCHART
Mirrorsfcc.id | gov | fccid.ai
Grantee Code2ASFG
Product CodeSONOCHART
Applicant BusinessCarestream Dental, LLC 🇺🇸
Related Domains csdental.com
Equipment ClassDental ultrasonic probe
Test Firmcetecom advanced GmbH

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2402-2480 MHzOriginal Equipment2024-08-08
5180-5240 MHzOriginal Equipment2024-08-08

Exhibits

DocumentTypeAvailableFile
User manual Part 1Users Manual2024-08-08PDF 1.2 MB
User manual Part 2Users Manual2024-08-08PDF 5.3 MB
Internal photosInternal Photos2024-08-08PDF 4.4 MB
External photosExternal Photos2024-08-08PDF 307.2 KB
LabelID Label/Location Info2024-08-08PDF 234.9 KB
Test_Setup_Photos_end_productTest Setup Photos2024-08-08PDF 344.9 KB
Test_Setup_Photos_moduleTest Setup Photos2024-08-08PDF 791.8 KB
Antenna informationTest Report2024-08-08PDF 2.1 MB
Test report SAR Part 1RF Exposure Info2024-08-08PDF 2.3 MB
Test report SAR Part 2RF Exposure Info2024-08-08PDF 3.1 MB
Test report SAR Part 3RF Exposure Info2024-08-08PDF 717.3 KB
Test_report_2G4WLAN_end_productTest Report2024-08-08PDF 893.1 KB
Test_report_2G4WLAN_module_Part_1Test Report2024-08-08PDF 3.9 MB
Test_report_2G4WLAN_module_Part_2Test Report2024-08-08PDF 4 MB
Test_report_2G4WLAN_module_Part_3Test Report2024-08-08PDF 4 MB
Test_report_2G4WLAN_module_Part_4Test Report2024-08-08PDF 2.9 MB
Test_report_5GWLAN_end_productTest Report2024-08-08PDF 813.5 KB
Test_report_5GWLAN_module_W161_Part_1Test Report2024-08-08PDF 5.9 MB
Test_report_5GWLAN_module_W161_Part_2Test Report2024-08-08PDF 5.7 MB
Test_report_5GWLAN_module_W166_Part_1Test Report2024-08-08PDF 5.4 MB
Test_report_5GWLAN_module_W166_Part_2Test Report2024-08-08PDF 3.8 MB
Test_report_Bluetooth_LE_end_productTest Report2024-08-08PDF 726.6 KB
2.911 letter Part 1Attestation Statements2024-08-08PDF 65.3 KB
2.911 letter Part 2Attestation Statements2024-08-08PDF 264.7 KB
LTCCover Letter(s)2024-08-08PDF 541.2 KB
Block diagram Metadata onlyBlock DiagramPDF 113.9 KB
Schematics end product Metadata onlySchematicsPDF 501.5 KB
Schematics module Metadata onlySchematicsPDF 813.8 KB
Operational description Metadata onlyOperational DescriptionPDF 233.5 KB
U-NII Declaration letter Metadata onlyOperational DescriptionPDF 1.8 MB
Software Security info Metadata onlySDR Software/Security Info.PDF 151.1 KB

Application Information

Application IDIVSRQwt+PJZ8Katu2yfrag==
Final Action Date2024-08-08
Application PurposeOriginal Equipment
Applicant FRN0028170819
ModelSONOCHART
Frequency Range2402-2480 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionDental ultrasonic probe
Responsible PartyKenneth Marshall, Radiation Safety Officer, Kenneth.Marshall@CSDental.com , 585-305-4261
Test FirmGerald Schmidt, cetecom advanced GmbH, tcb@cetecomadvanced.com , 49-681-598-0
TCB Emailtcb@cetecomadvanced.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityYes
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceYes
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsOutput power listed is peak conducted for BTLE and average conducted for WLAN. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz bandwidth and a 40 MHz bandwidth mode. This device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for extremities and body-worn SAR exposure conditions are 0.01 W/kg and 0.06 W/kg, respectively.

Applications

Application IDDatePurpose
IVSRQwt+PJZ8Katu2yfrag==2024-08-08Original Equipment
6659Buu0NmbAsmRICH9YUQ==2024-08-08Original Equipment

Equipment Authorization

FrequencyOutputRulesGrant Notes
2402-2480 MHz0.0060315CCC
2412-2462 MHz0.05815CCC
5180-5240 MHz0.052515ECC
5260-5320 MHz0.052515ECC
5500-5700 MHz0.061715ECC
5745-5825 MHz0.060315ECC

Grants

TCB Grant - Application IVSRQwt+PJZ8Katu2yfrag==

TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  cetecom advanced GmbH
Untertuerkheimer Strasse 6-10
Saarbruecken, 66117
Germany
Date of Grant: 08/08/2024

Application Dated: 08/08/2024
Carestream Dental, LLC
3625 Cumberland Ave Suite 700
Atlanta, GA 30339
 
Attention: Kenneth Marshall , Radiation Safety Officer

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  2ASFG-SONOCHART
Name of Grantee:  Carestream Dental, LLC
Equipment Class: Digital Transmission System
Notes: Dental ultrasonic probe
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2402.0  -  2480.0 0.00603  
CC 15C 2412.0  -  2462.0 0.058  

Output power listed is peak conducted for BTLE and average conducted for WLAN. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz bandwidth and a 40 MHz bandwidth mode. This device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for extremities and body-worn SAR exposure conditions are 0.01 W/kg and 0.06 W/kg, respectively.

CC: This device is certified pursuant to two different Part 15 rules sections.

EAS Grant - Application IVSRQwt+PJZ8Katu2yfrag==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Carestream Dental, LLC
3625 Cumberland Ave Suite 700
Atlanta, GA 30339
United States
  Date of Grant: 08/08/2024

Application Dated: 08/08/2024
 
Attention: Kenneth Marshall , Radiation Safety Officer

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  2ASFG-SONOCHART
Name of Grantee:  Carestream Dental, LLC
Equipment Class: Digital Transmission System
Notes: Dental ultrasonic probe
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2402.0  -  2480.0 0.00603  
CC 15C 2412.0  -  2462.0 0.058  

Output power listed is peak conducted for BTLE and average conducted for WLAN. This device supports IEEE 802.11b (Wi-Fi 1) with a 20 MHz bandwidth mode, IEEE 802.11g (Wi-Fi 3) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz bandwidth and a 40 MHz bandwidth mode. This device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for extremities and body-worn SAR exposure conditions are 0.01 W/kg and 0.06 W/kg, respectively.


CC: This device is certified pursuant to two different Part 15 rules sections.

TCB Grant - Application 6659Buu0NmbAsmRICH9YUQ==

Mail To:
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  cetecom advanced GmbH
Untertuerkheimer Strasse 6-10
Saarbruecken, 66117
Germany
Date of Grant: 08/08/2024

Application Dated: 08/08/2024
Carestream Dental, LLC
3625 Cumberland Ave Suite 700
Atlanta, GA 30339
 
Attention: Kenneth Marshall , Radiation Safety Officer

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  2ASFG-SONOCHART
Name of Grantee:  Carestream Dental, LLC
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: Dental ultrasonic probe
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15E 5180.0  -  5240.0 0.0525  
CC 15E 5260.0  -  5320.0 0.0525  
CC 15E 5500.0  -  5700.0 0.0617  
CC 15E 5745.0  -  5825.0 0.0603  

Output power listed is average conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz bandwidth and a 40 MHz bandwidth mode. The device is a client device only. This device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for extremities and body-worn SAR exposure conditions are 0.05 W/kg and 0.28 W/kg, respectively.

CC: This device is certified pursuant to two different Part 15 rules sections.

EAS Grant - Application 6659Buu0NmbAsmRICH9YUQ==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Carestream Dental, LLC
3625 Cumberland Ave Suite 700
Atlanta, GA 30339
United States
  Date of Grant: 08/08/2024

Application Dated: 08/08/2024
 
Attention: Kenneth Marshall , Radiation Safety Officer

NOT TRANSFERABLE
EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.
 
FCC IDENTIFIER:  2ASFG-SONOCHART
Name of Grantee:  Carestream Dental, LLC
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: Dental ultrasonic probe
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15E 5180.0  -  5240.0 0.0525  
CC 15E 5260.0  -  5320.0 0.0525  
CC 15E 5500.0  -  5700.0 0.0617  
CC 15E 5745.0  -  5825.0 0.0603  

Output power listed is average conducted. This device supports IEEE 802.11a (Wi-Fi 2) with a 20 MHz bandwidth mode and IEEE 802.11n (Wi-Fi 4) with a 20 MHz bandwidth and a 40 MHz bandwidth mode. The device is a client device only. This device has been tested touched to the phantom and meets FCC RF exposure guidelines. The highest reported SAR for extremities and body-worn SAR exposure conditions are 0.05 W/kg and 0.28 W/kg, respectively.


CC: This device is certified pursuant to two different Part 15 rules sections.

Mail To: