Vygon 1212.08

by VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number03660812011303 UDI-DI	Date26 Mar 2018Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Vygon
Generic Name: Centrally-inserted central venous catheter
Model / Ref / Catalog: 1212.08

Primary DI / UDI-DI: 03660812011303
FDA Product Code: FOZ
GMDN Term: Centrally-inserted central venous catheter

Device Class: Class II
Regulation Number: 880.5200
GUDID distribution status: In Commercial Distribution

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Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (7)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No