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Vygon

FDA UDI

Class I (US FDA UDI)

by Vygon Corp.

Identity

Trade Name
VYGON FDA UDI
Generic Name
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI
Device Name
Vyconnector - ØExt. 7.0-9.5mm / 7.0-9.5mm FDA UDI
Model / Reference
881.77 FDA UDI
Description
Vyconnector - ØExt. 7.0-9.5mm / 7.0-9.5mm FDA UDI

Identifiers

Catalog Number
00088177 FDA UDI
Primary DI / UDI-DI
03660812134538 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-ISO80369-standardized small-bore linear connector, single-use

Vygon by Vygon Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-ISO80369-standardized small-bore linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vygon Corp.

Sources (1)

  • FDA UDI f646230a-7db4-4e3d-b2cf-70ecc48a6393 35 fields · synced Jun 6, 2026