Vygon

FDA UDI

Class II (US FDA UDI)

by Vygon Corp.

Identity

Trade Name: VYGON FDA UDI
Generic Name: Intrathecal anaesthesia set, non-medicated FDA UDI
Device Name: NERVE BLOCK CATHETER KIT FDA UDI
Model / Reference: AMS-9059CP FDA UDI
Description: NERVE BLOCK CATHETER KIT FDA UDI

Identifiers

Catalog Number: AMS-9059CP FDA UDI
Primary DI / UDI-DI: 00849884003383 FDA UDI
FDA Product Code: OGJ FDA UDI
GMDN Term: Intrathecal anaesthesia set, non-medicated FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5140 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Intrathecal anaesthesia set, non-medicated

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Vygon Corp.

Sources (1)

FDA UDI 7d0a4389-e0cd-4cda-9f0b-b9919c8a4ce0 34 fields · synced Jun 1, 2026