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TEWA PB-Type 2025

by asia-med GmbH

TEWA PB-Type 2025 (A000696) is an acupuncture needle (FDA Class II; FDA product code MQX, Needle, Acupuncture, Single Use) made by asia-med GmbH, listed in FDA GUDID since 30 Nov 2017 (UDI-DI 04251282512552), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04251282512552 UDI-DI Date30 Nov 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  • Withdrawn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
Tewa
Generic name
Acupuncture needle, single-use
Model / Ref / Catalog
PB-Type 2025, A000696
Primary DI / UDI-DI
04251282512552
FDA product code
MQX
GMDN term
Acupuncture needle, single-use
Device class
Class II
Regulation number
880.5580
GUDID distribution status
In Commercial Distribution
Size
Length — 25 Millimeter
Outer Diameter — 0.20 Millimeter

Similar devices in this category

Other devices filed under Acupuncture needle, single-use.

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Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)