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Vesco Medical

FDA UDI

Class II (US FDA UDI)

by Vesco Medical Llc

Identity

Trade Name
Vesco Medical FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
10mL ENFit Multifil Enteral Feeding Syringe FDA UDI
Model / Reference
VED-610R FDA UDI
Description
10mL ENFit Multifil Enteral Feeding Syringe FDA UDI

Identifiers

Catalog Number
VED-610R FDA UDI
Primary DI / UDI-DI
00810096151193 FDA UDI
510(k) Number
K222155 FDA UDI
FDA Product Code
PNR FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 10 Milliliter FDA UDI

Category: ENFit oral/enteral syringe, single-use

Vesco Medical by Vesco Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

Cleared under the same submission

K222155 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vesco Medical Llc

Sources (1)

  • FDA UDI c58d3591-a32b-4705-af39-66cabdcc57cb 37 fields · synced May 30, 2026