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Demax DPY04B

by Beijing Demax Medical Technology Co., Ltd.

Demax DPY04B is a Class II device made by Beijing Demax Medical Technology Co., Ltd., listed in FDA GUDID since 14 Jul 2022 (UDI-DI 06943718213109), 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 Number06943718213109 UDI-DI Date14 Jul 2022ListedStatusListed 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  • Withdrawn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
Demax
Generic name
Haemostasis valve
Model / reference
DPY04B
Primary DI / UDI-DI
06943718213109
FDA product code
DTL
GMDN term
Haemostasis valve
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemostasis valve

Similar devices in this category

Other devices filed under Haemostasis valve.

Other devices from Beijing Demax Medical Technology Co., Ltd.

See all devices from Beijing Demax Medical Technology Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)