← Back to catalogue

V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Endoscope antifog solution FDA UDI
Device Name
V. Mueller PREMIUM ANTI-FOG WITH FLIP TOP BOTTLE 20 EACH/BOX FDA UDI
Model / Reference
LAFOG-FT FDA UDI
Description
V. Mueller PREMIUM ANTI-FOG WITH FLIP TOP BOTTLE 20 EACH/BOX FDA UDI

Identifiers

Catalog Number
LAFOGFT FDA UDI
Primary DI / UDI-DI
10885403231643 FDA UDI
FDA Product Code
OCT FDA UDI
GMDN Term
Endoscope antifog solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope antifog solution

V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope antifog solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 40cd392c-b027-4133-bae5-6051fe3017a8 35 fields · synced Jun 8, 2026