Anti-fog w/Pad

FDA UDI

Class II (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name: Anti-fog w/Pad FDA UDI
Generic Name: Endoscope antifog solution FDA UDI
Model / Reference: 30910 FDA UDI

Identifiers

Primary DI / UDI-DI: 20787551000096 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

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 by Xodus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 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 d080f19e-7460-4cc8-b795-59b357f7b197 33 fields · synced May 30, 2026