Trigen E0017169-7

by Smith & Nephew, Inc.

Trigen E0017169-7 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 17 Nov 2020 (UDI-DI 00885556799369), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00885556799369 UDI-DI	Date17 Nov 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00885556799369

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trigen
Generic name: Bone awl, reusable
Model / Ref / Catalog: E0017169-7

Primary DI / UDI-DI: 00885556799369
FDA product code: HWJ
GMDN term: Bone awl, reusable

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)