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Numobag Kit NBC952

by Numotech, Inc.

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

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 Number00860010630600 UDI-DI Date11 Jul 2023ListedStatusListed GUDID: 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  • Withdrawn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
Numobag Kit
Generic Name
Extremity-oxygenation hyperbaric chamber, non-powered
Model / Reference
NBC952
Primary DI / UDI-DI
00860010630600
FDA Product Code
KPJ
GMDN Term
Extremity-oxygenation hyperbaric chamber, non-powered
Device Class
Class II
Regulation Number
878.5650
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Extremity-oxygenation hyperbaric chamber, non-powered

Other devices from Numotech, Inc.

Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No