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05.001.183

by Synthes GmbH

05.001.183 (05001183) is a Class II device made by Synthes GmbH, listed in FDA GUDID since 30 Jun 2016 (UDI-DI 10886982129567), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10886982129567 UDI-DI Date30 Jun 2016ListedStatusListed 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  • Withdrawn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
Sawing power tool attachment, sagittal
Model / Ref / Catalog
05.001.183, 05001183
Primary DI / UDI-DI
10886982129567
FDA product code
HBB, HWE, HBE, ERL, DZI
GMDN term
Sawing power tool attachment, sagittal
Device class
Class II
Regulation number
882.4370, 878.4820, 882.4310, 874.4250, 872.4120
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Sawing power tool attachment, sagittal

Similar devices in this category

Other devices filed under Sawing power tool attachment, sagittal.

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See all devices from Synthes GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)