Afp 810

FDA UDI

Class II (US FDA UDI)

by Afp Manufacturing, Inc.

Identity

Trade Name: AFP 810 FDA UDI
Generic Name: Dental automated x-ray film processor FDA UDI
Device Name: x-ray film processor, dental FDA UDI
Model / Reference: AFP 810 Basic FDA UDI
Description: x-ray film processor, dental FDA UDI

Identifiers

Catalog Number: 2001 FDA UDI
Primary DI / UDI-DI: B580EGY0 FDA UDI
FDA Product Code: EGY FDA UDI
GMDN Term: Dental automated x-ray film processor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental automated x-ray film processor

Afp 810 by Afp Manufacturing, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental automated x-ray film processor.

Peri-Pro III Intraoral Film Processor — Air Techniques, Inc. · Class II
ExtraXtender Film Processor — MEDIVANCE INSTRUMENTS LIMITED · Class II
IntraX Film Processor — MEDIVANCE INSTRUMENTS LIMITED · Class II
A/T 2000 XR Intraoral Film Processor — Air Techniques, Inc. · Class II
A/T 2000 XR Intraoral Film Processor with Water Recirculation System — Air Techniques, Inc. · Class II
Mini Med — AFP MANUFACTURING, INC. · Class II

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: Afp Manufacturing, Inc.

Sources (1)

FDA UDI 3126e00d-0516-4ee0-94e1-c1edff746f3a 34 fields · synced May 30, 2026