Peri-Pro III Intraoral Film Processor

FDA UDI

Class II (US FDA UDI)

by Air Techniques, Inc.

Identity

Trade Name: Peri-Pro III Intraoral Film Processor FDA UDI
Generic Name: Dental automated x-ray film processor FDA UDI
Device Name: Peri-Pro III Intraoral Film Processor is a roller-less transport system that guides up to eight films at once through the developing process. The films are processed, dried with heated air, and deposited into the film receptacle dry-to dry and ready to read. Includes: 1 case chemistry, film carriers: 3 Pedo film carriers, 2 adult anterior film carriers, 2 bite-wing film carriers, 1 occlusal film carrier, 1 water bottle. FDA UDI
Model / Reference: 94000 FDA UDI
Description: Peri-Pro III Intraoral Film Processor is a roller-less transport system that guides up to eight films at once through the developing process. The films are processed, dried with heated air, and deposited into the film receptacle dry-to dry and ready to read. Includes: 1 case chemistry, film carriers: 3 Pedo film carriers, 2 adult anterior film carriers, 2 bite-wing film carriers, 1 occlusal film carrier, 1 water bottle. FDA UDI

Identifiers

Primary DI / UDI-DI: D678940000 FDA UDI
FDA Product Code: IXW 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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Weight — 22 Pound FDA UDI
Depth — 10 Inch FDA UDI
Width — 25 Inch FDA UDI
Height — 8.5 Inch FDA UDI

Category: Dental automated x-ray film processor

Peri-Pro III Intraoral Film Processor by Air Techniques, 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: Air Techniques, Inc.

Sources (1)

FDA UDI 6ff1cdd6-09d5-4991-a265-9618be1ad4a3 36 fields · synced Jun 9, 2026