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Baum 1051NL

by W.A. Baum Co., Inc.

Baum 1051NL is a Class II device made by W.A. Baum Co., Inc., listed in FDA GUDID since 1 Oct 2019 (UDI-DI 00810010920249), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810010920249 UDI-DI Date1 Oct 2019ListedStatusListed 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  • Withdrawn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
Baum
Generic name
Aneroid manual sphygmomanometer
Model / Ref / Catalog
1051NL
Primary DI / UDI-DI
00810010920249
FDA product code
DXN
GMDN term
Aneroid manual sphygmomanometer
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometer

Other devices from W.A. Baum Co., Inc.

See all devices from W.A. Baum Co., Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)