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Codman

FDA UDI

Class I (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
CODMAN SLIM-LINE MICROCARE Aneurysm Clip Tray No 3 FDA UDI
Model / Reference
80-1843 FDA UDI
Description
CODMAN SLIM-LINE MICROCARE Aneurysm Clip Tray No 3 FDA UDI

Identifiers

Catalog Number
801843 FDA UDI
Primary DI / UDI-DI
10886704037965 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Codman by Cerenovus, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cerenovus, Inc.

Sources (1)

  • FDA UDI 32688927-f181-459d-a094-dddaf7503710 36 fields · synced May 31, 2026