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Vygon

FDA UDI

Class II (US FDA UDI)

by Vygon Corp.

Identity

Trade Name
VYGON FDA UDI
Generic Name
Vascular catheter introduction needle FDA UDI
Device Name
24GA. CANNULA INTRODUCER FDA UDI
Model / Reference
CMS-207 FDA UDI
Description
24GA. CANNULA INTRODUCER FDA UDI

Identifiers

Catalog Number
CMS-207 FDA UDI
Primary DI / UDI-DI
00849884003949 FDA UDI
510(k) Number
K954302 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Vascular catheter introduction needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular catheter introduction needle

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

Similar devices

Also classified as Vascular catheter introduction needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vygon Corp.

Sources (1)

  • FDA UDI 4e37cdbc-661d-4f3f-97a1-451d4e024595 35 fields · synced May 30, 2026