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Antmed PT182203

by ShenZhen Antmed Co., Ltd

Antmed PT182203 is a Class II device made by ShenZhen Antmed Co., Ltd, listed in FDA GUDID since 25 Aug 2017 (UDI-DI 06945764415766), 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 Number06945764415766 UDI-DI Date25 Aug 2017ListedStatusListed 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  • Withdrawn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
Antmed
Generic name
Invasive blood pressure transducer set
Model / reference
PT182203
Primary DI / UDI-DI
06945764415766
FDA product code
DRS
GMDN term
Invasive blood pressure transducer set
Device class
Class II
Regulation number
870.2850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Invasive blood pressure transducer set

Similar devices in this category

Other devices filed under Invasive blood pressure transducer set.

Other devices from ShenZhen Antmed Co., Ltd

See all devices from ShenZhen Antmed Co., Ltd →

Properties

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