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Vesco

FDA UDI

Class I (US FDA UDI)

by Ucomfor Scientific Co., Ltd

Identity

Trade Name
VESCO FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
PVC Enteral Drainage Bag 500mL FDA UDI
Model / Reference
VED-010EO FDA UDI
Description
PVC Enteral Drainage Bag 500mL FDA UDI

Identifiers

Primary DI / UDI-DI
06972261829055 FDA UDI
FDA Product Code
FFD FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4370 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Closed-wound/centesis drainage receptacle

Vesco by Ucomfor Scientific Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound/centesis drainage receptacle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 62f668a7-4972-4dd3-b12c-4e753643ddee 33 fields · synced May 30, 2026