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Vygon 542.12

by Vygon

Vygon 542.12 is a Class I device made by Vygon, listed in FDA GUDID since 27 Feb 2018 (UDI-DI 33660812006911), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number33660812006911 UDI-DI Date27 Feb 2018ListedStatusListed 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  • Withdrawn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
Vygon
Generic name
General specimen container IVD, no additive, sterile
Model / Ref / Catalog
542.12
Primary DI / UDI-DI
33660812006911
FDA product code
BSY
GMDN term
General specimen container IVD, no additive, sterile
Device class
Class I
Regulation number
868.6810
GUDID distribution status
In Commercial Distribution

Related devices

Category: General specimen container IVD, no additive, sterile

Similar devices in this category

Other devices filed under General specimen container IVD, no additive, sterile.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)