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/ 500cc

by Suzhou Minhua Medical Apparatus Supplies Co., Ltd. 3 variants

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 Number06971996174355 UDI-DI Date2 Sep 2026ListedStatusListed 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  • Withdrawn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
/
Generic Name
Intravenous pressure infusor, manual, reusable
Model / Reference
500cc
Primary DI / UDI-DI
06971996174355
FDA Product Code
KZD
GMDN Term
Intravenous pressure infusor, manual, reusable
Device Class
Class I
Regulation Number
880.5420
GUDID distribution status
In Commercial Distribution

Other devices from Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

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Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No