← Back to catalogue

Emergency Response Kit

FDA UDI

Class I (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
Emergency Response Kit FDA UDI
Generic Name
Cardiopulmonary resuscitation kit, single-use FDA UDI
Device Name
Emergency Response Kit FDA UDI
Model / Reference
11998 FDA UDI
Description
Emergency Response Kit FDA UDI

Identifiers

Catalog Number
11998-000334 FDA UDI
Primary DI / UDI-DI
00883873772676 FDA UDI
FDA Product Code
PXD FDA UDI
GMDN Term
Cardiopulmonary resuscitation kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary resuscitation kit, single-use

Emergency Response Kit by PHYSIO-CONTROL, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary resuscitation kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ffa63a1e-11f4-474d-823e-688b2745f1d2 36 fields · synced Jun 9, 2026