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Hillrom™ 2069351

by Baxter Medical Systems GmbH + Co. KG

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887761979901 UDI-DI Date20 Aug 2021ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hillrom™
Generic Name
Operating table orthopaedic extension, non-powered
Model / Reference
2069351
Primary DI / UDI-DI
00887761979901
FDA Product Code
JEA, KXJ, GDC
GMDN Term
Operating table orthopaedic extension, non-powered
Device Class
Class I
Regulation Number
878.4960, 892.1980
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No