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Codman Sofwire

FDA UDI

Class I (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN SOFWIRE FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
CODMAN SOF'WIRE Cable Instrument Tray FDA UDI
Model / Reference
464011 FDA UDI
Description
CODMAN SOF'WIRE Cable Instrument Tray FDA UDI

Identifiers

Catalog Number
464011 FDA UDI
Primary DI / UDI-DI
10705034002231 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, 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

Codman Sofwire 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 28fd7f6e-a500-4efb-a6b1-52b08cd5bc54 36 fields · synced Jun 8, 2026