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Anthem 1181.2412

by Globus Medical, Inc.

Anthem 1181.2412 is a Class II device made by Globus Medical, Inc., listed in FDA GUDID since 25 Nov 2021 (UDI-DI 00193982334024), 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 Number00193982334024 UDI-DI Date25 Nov 2021ListedStatusListed 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  • Withdrawn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

Trade name
Anthem
Generic name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile
Model / reference
1181.2412
Primary DI / UDI-DI
00193982334024
FDA product code
HWC, HRS
GMDN term
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile
Device class
Class II
Regulation number
888.3040, 888.3030
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Similar devices in this category

Other devices filed under Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile.

Other devices from Globus Medical, Inc.

See all devices from Globus Medical, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Lot / batch number
Other properties (12, all answered No)