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Codman®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
CODMAN® FDA UDI
Generic Name
Scalp haemostasis clip, reusable FDA UDI
Device Name
CODMAN® RANEY Scalp Clips FDA UDI
Model / Reference
201025 FDA UDI
Description
CODMAN® RANEY Scalp Clips FDA UDI

Identifiers

Catalog Number
20-1025 FDA UDI
Primary DI / UDI-DI
10381780511588 FDA UDI
FDA Product Code
HBO FDA UDI
GMDN Term
Scalp haemostasis clip, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4150 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Scalp haemostasis clip, reusable

Codman® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalp haemostasis clip, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd9a930a-65c0-4102-bc4c-c3dd92f7570d 35 fields · synced Jun 9, 2026