← Back to catalogue

A/T 2000 XR Intraoral Film Processor with Water Recirculation System

FDA UDI

Class II (US FDA UDI)

by Air Techniques, Inc.

Identity

Trade Name
A/T 2000 XR Intraoral Film Processor with Water Recirculation System FDA UDI
Generic Name
Dental automated x-ray film processor FDA UDI
Device Name
A/T 2000 XR Intraoral Film Processor with Water Recirculation System provides high quality radiographs in any size such as Panoramic, Cephalometric, TMJ, Occlusal and all Intraorals. Includes: 1 levelling base, 1 bottle spray 2000 Plus; 4 Air Techniques cleaning films; 1 instructional DVD: 1 case chemistry, 1 bottle of starter, and 2 1/2 gallon water container. FDA UDI
Model / Reference
45004 FDA UDI
Description
A/T 2000 XR Intraoral Film Processor with Water Recirculation System provides high quality radiographs in any size such as Panoramic, Cephalometric, TMJ, Occlusal and all Intraorals. Includes: 1 levelling base, 1 bottle spray 2000 Plus; 4 Air Techniques cleaning films; 1 instructional DVD: 1 case chemistry, 1 bottle of starter, and 2 1/2 gallon water container. FDA UDI

Identifiers

Primary DI / UDI-DI
D678450040 FDA UDI
510(k) Number
K001321 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 75 Pound FDA UDI
Depth — 26 Inch FDA UDI
Width — 14.25 Inch FDA UDI
Height — 15 Inch FDA UDI

Category: Dental automated x-ray film processor

A/T 2000 XR Intraoral Film Processor with Water Recirculation System by Air Techniques, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental automated x-ray film processor.

Cleared under the same submission

K001321 also covers:

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
Air Techniques, Inc.

Sources (1)

  • FDA UDI fb155152-f60c-45d9-a1f8-01e7524b35ee 37 fields · synced Jun 9, 2026