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4100125000

by Stryker Corp.

4100125000 (4100-125-000) is a Class I device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540068163), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04546540068163 UDI-DI Date24 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Pin-driving power tool attachment
Model / Ref / Catalog
4100125000, 4100-125-000
Primary DI / UDI-DI
04546540068163
FDA product code
HWE
GMDN term
Pin-driving power tool attachment
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Pin-driving power tool attachment

Similar devices in this category

Other devices filed under Pin-driving power tool attachment.

Other devices from Stryker Corp.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)