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CodeManagement Module®

FDA UDI

Class II (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
CodeManagement Module® FDA UDI
Generic Name
Physiologic-monitoring defibrillation system FDA UDI
Device Name
ASSEMBLY - CODE MANAGEMENT MODULE, WI-FI AND CO2 FDA UDI
Model / Reference
11150 FDA UDI
Description
ASSEMBLY - CODE MANAGEMENT MODULE, WI-FI AND CO2 FDA UDI

Identifiers

Catalog Number
11150-000017 FDA UDI
Primary DI / UDI-DI
00883873892701 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Physiologic-monitoring defibrillation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Physiologic-monitoring defibrillation system

CodeManagement Module® by PHYSIO-CONTROL, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physiologic-monitoring defibrillation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI f3091a25-168a-43ad-b159-9f7742660955 35 fields · synced Jun 9, 2026