Anti-Fog w/ Pad +1 more model

FDA UDI

Class II (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name: Anti-Fog w/ Pad; in Tray FDA UDI
Generic Name: Endoscope antifog solution FDA UDI
Model / Reference: 30900TR FDA UDI

Identifiers

Primary DI / UDI-DI: 20787551000034 FDA UDI
FDA Product Code: OCT FDA UDI
GMDN Term: Endoscope antifog solution FDA UDI
Models / Variants: Anti-Fog w/ Pad FDA UDI
in Tray 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Endoscope antifog solution

Anti-Fog w/ Pad +1 more model by Xodus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Xodus Medical, Inc.

Sources (1)

FDA UDI fefdd767-e571-4241-9b24-22013eb2877c 33 fields · synced Jun 1, 2026