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Vilex EPF/MEND Endoscopy Systems

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Vilex EPF/MEND Endoscopy Systems FDA UDI
Generic Name
Hand-held endoscopic retractor, reusable FDA UDI
Device Name
Spreader, EPF/MEND FDA UDI
Model / Reference
Y206 FDA UDI
Description
Spreader, EPF/MEND FDA UDI

Identifiers

Catalog Number
Y206 FDA UDI
Primary DI / UDI-DI
00841731138057 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Hand-held endoscopic retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held endoscopic retractor, reusable

Vilex EPF/MEND Endoscopy Systems by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held endoscopic retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI 92f0a15e-257a-4093-91b8-f23a52338eef 34 fields · synced May 30, 2026