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Codman®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
CODMAN® FDA UDI
Generic Name
Subcutaneous tunneller, single-use FDA UDI
Device Name
CODMAN® Peel-Away Catheter Introducer FDA UDI
Model / Reference
831326 FDA UDI
Description
CODMAN® Peel-Away Catheter Introducer FDA UDI

Identifiers

Catalog Number
83-1326 FDA UDI
Primary DI / UDI-DI
10381780537410 FDA UDI
510(k) Number
K883607 FDA UDI
FDA Product Code
GYK FDA UDI
GMDN Term
Subcutaneous tunneller, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4545 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 14 French FDA UDI

Category: Subcutaneous tunneller, single-use

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

Similar devices

Also classified as Subcutaneous tunneller, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22c89c77-25e6-4cd3-af7b-fa2de0b5bb10 37 fields · synced Jun 9, 2026