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Trigen

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TRIGEN FDA UDI
Generic Name
Medical capital equipment storage bag/case FDA UDI
Device Name
TRAUMA INTERFACE CASE - 2ND GENERATION FDA UDI
Model / Reference
71692857 FDA UDI
Description
TRAUMA INTERFACE CASE - 2ND GENERATION FDA UDI

Identifiers

Catalog Number
71692857 FDA UDI
Primary DI / UDI-DI
00885556584675 FDA UDI
510(k) Number
K170977 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Medical capital equipment storage bag/case FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

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

Category: Medical capital equipment storage bag/case

Trigen by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical capital equipment storage bag/case.

Cleared under the same submission

K170977 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e005e6de-aeae-4016-89a6-0bb23b9dca23 36 fields · synced Jun 8, 2026