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Vygon

FDA UDI

Class II (US FDA UDI)

by Vygon Corp.

Identity

Trade Name
VYGON FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
Nutrisafe2 Y Connector with Oral Port FDA UDI
Model / Reference
368.42R FDA UDI
Description
Nutrisafe2 Y Connector with Oral Port FDA UDI

Identifiers

Catalog Number
368.42R FDA UDI
Primary DI / UDI-DI
00849884002393 FDA UDI
510(k) Number
K060944 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric feeding tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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: Nasogastric feeding tube

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

Similar devices

Also classified as Nasogastric feeding tube.

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 912e03af-bffc-4378-a874-870491c75878 35 fields · synced Jun 8, 2026