← Back to catalogue

Vygon

FDA UDI

Class II (US FDA UDI)

by Vygon Corp.

Identity

Trade Name
VYGON FDA UDI
Generic Name
Haemodialysis/central venous catheterization kit FDA UDI
Device Name
MIDLINE CATHETER PREP TRAY FDA UDI
Model / Reference
AMS-8186CP FDA UDI
Description
MIDLINE CATHETER PREP TRAY FDA UDI

Identifiers

Catalog Number
AMS-8186CP FDA UDI
Primary DI / UDI-DI
00849884003154 FDA UDI
FDA Product Code
OFK FDA UDI
GMDN Term
Haemodialysis/central venous catheterization kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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: Haemodialysis/central venous catheterization kit

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

Similar devices

Also classified as Haemodialysis/central venous catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Vygon Corp.

Sources (1)

  • FDA UDI 0c675f42-4841-4114-9294-0d56c6f97012 34 fields · synced May 30, 2026