FCC ID 2ABS9RADIO1

2ABS9-RADIO1, 2ABS9 RADIO1, 2ABS9RADI01, 2ABS9RADIO1, 2ABS9RADIOI, 2ABS9RAD1O1, 2AB59RADIO1

CRISI Medical Systems Manual Injection monitoring system for anesthesia RADIO1

An FCC ID is the product ID assigned by the FCC to identify wireless products in the market. The FCC chooses 3 or 5 character "Grantee" codes to identify the business that created the product. For example, the grantee code for FCC ID: 2ABS9RADIO1 is 2ABS9. The remaining characters of the FCC ID, RADIO1, are often associated with the product model, but they can be random. These letters are chosen by the applicant. In addition to the application, the FCC also publishes internal images, external images, user manuals, and test results for wireless devices. They can be under the "exhibits" tab below.

Purchase on Amazon: Manual Injection monitoring system for anesthesia

Application: Manual Injection monitoring system for anesthesia
Equipment Class: DXX - Part 15 Low Power Communication Device Transmitter
Short Link: fcc.id/2ABS9RADIO1
Sources: FCC.gov | FCC.report
Registered By: CRISI Medical Systems - 2ABS9 (United States)

App #	Purpose	Date	Unique ID
1	Original Equipment	2014-03-06	sTs83DavOPVvIeO/ckAc8w==

Operating Frequencies

Frequency Range	Rule Parts	Line Entry
2.402-2.48 GHz	15C	1

Exhibits

Document	Type	Submitted Available
User Manual	Users Manual Adobe Acrobat PDF (2577 kB)	2014-03-06 2014-03-06
Test Report	Test Report Adobe Acrobat PDF (205 kB)	2014-03-06 2014-03-06
Set Up Photos	Test Setup Photos Adobe Acrobat PDF (370 kB)	2014-03-06 2014-03-06
Label	ID Label/Location Info Adobe Acrobat PDF (199 kB)	2014-03-06 2014-03-06
Internal Photos	Internal Photos Adobe Acrobat PDF (133 kB)	2014-03-06 2014-03-06
External Photos	External Photos Adobe Acrobat PDF (190 kB)	2014-03-06 2014-03-06
Cover Letter	Cover Letter(s) Adobe Acrobat PDF (114 kB)	2014-03-06 2014-03-06
Operational Description	Operational Description Adobe Acrobat PDF (820 kB)	2014-03-06
Schematics	Schematics Adobe Acrobat PDF (124 kB)	2014-03-06
Block Diagram	Block Diagram Adobe Acrobat PDF (221 kB)	2014-03-06
Parts List	Parts List/Tune Up Info Adobe Acrobat PDF (18 kB)	2014-03-06

Application Forms

1 (2014-03-06)

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	CRISI Medical Systems
FCC Registration Number (FRN):	0023326200
Alphanumeric FCC ID:	2ABS9RADIO1
Unique Application Identifier:	sTs83DavOPVvIeO/ckAc8w==
Line one:	9191 Towne Centre Drive, Ste. 330
Line two:	9191 Towne Centre Drive, Ste. 330
City:	San Diego
State:	California
Country:	United States
Zip Code:	92122

TCB Information

TCB Application Email Address:	stuart.beck@nemko.com
TCB Scope:	A2: Low Power Transmitters (except Spread Spectrum) and radar detectors operating above 1 GHz

FCC ID

Grantee Code:	2ABS9
Product Code:	RADIO1

Person at the applicant's address to receive grant or for contact

Name:	Walter Bochenko
Title:	VP Product Development

Telephone Number:

7605058752

Extension:

Fax Number:	none
Email:	wbochenko@crisimed.com

Long-Term Confidentiality

Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: Yes

Short-Term Confidentiality

Does short-term confidentiality apply to this application?: No

If so, specify the short-term confidentiality release date (MM/DD/YYYY format):
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio

Is this application for software defined/cognitive radio authorization? No

Equipment Class

Equipment Class: DXX - Part 15 Low Power Communication Device Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant):	Manual Injection monitoring system for anesthesia

Related OET KnowledgeDataBase Inquiry

Is there a KDB inquiry associated with this application? No

Modular Equipment

Modular Type: Does not apply

Application Purpose

Application is for: Original Equipment

Composite/Related Equipment

Is the equipment in this application a composite device subject to an additional equipment authorization? Yes

Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization? Yes

Test Firm Information

Name of test firm and contact person on file with the FCC:

Firm Name: Nemko USA, Inc. - San Diego EMC Division

First Name: Jim

Last Name: Morris

Telephone Number:

760-444-3401

Extension:

Fax Number: 760-444-3505

E-mail: Jim.Morris@nemko.com

Grant Comments

Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver

Is there an equipment authorization waiver associated with this application? No

If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?: No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:

The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify? Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing: Alan Laudani

Title of authorized signature: Senior RF/EMC Test Engineer

Complete items below if agent signs the application:

Firm Name: Nemko USA

Name: Alan Alan Alan

Line 1: Alan

Line 2: Alan

P.O. Box: Alan

City: Alan

State: Alan

Country: Alan

Zip Code: Alan

E-mail: alan.laudani@nemko.com

Applications are submitted for FCC ID and Grant requests. Click an above application to view details

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

Nemko Canada Inc.
303 River Road
Ottawa, Ontario, K1V 1H2
Canada

Date of Grant: 03/06/2014

Application Dated: 03/06/2014

CRISI Medical Systems

9191 Towne Centre Drive, Ste. 330

San Diego, CA 92122

Attention: Walter Bochenko , VP Product Development

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:	2ABS9RADIO1

Name of Grantee:	CRISI Medical Systems

Equipment Class:	Part 15 Low Power Communication Device Transmitter
Notes:	Manual Injection monitoring system for anesthesia

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	15C	2402.0 - 2480.0

COPY	FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION	COPY
Certification

CRISI Medical Systems
9191 Towne Centre Drive, Ste. 330 9191 Towne Centre Drive, Ste. 330
San Diego, CA 92122
United States