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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
Epidural needle, non-threaded FDA UDI
Device Name
CODMAN® Tuohy Needle FDA UDI
Model / Reference
451020 FDA UDI
Description
CODMAN® Tuohy Needle FDA UDI

Identifiers

Catalog Number
45-1020 FDA UDI
Primary DI / UDI-DI
10381780514268 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Epidural needle, non-threaded FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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: Epidural needle, non-threaded

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

Similar devices

Also classified as Epidural needle, non-threaded.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 637613df-7efa-42a5-973c-dc9cf18b82dd 35 fields · synced Jun 9, 2026