Identity
- Trade Name
- Plate Transfer Box FDA UDI
- Generic Name
- Digital imaging cassette FDA UDI
- Device Name
- An accessory that protects the PSP during typical day-to-day use and storage. The transfer box also protects the PSP image against light source damage when they are moved from the patient to the unit. FDA UDI
- Model / Reference
- 73470 FDA UDI
- Description
- An accessory that protects the PSP during typical day-to-day use and storage. The transfer box also protects the PSP image against light source damage when they are moved from the patient to the unit. FDA UDI
Identifiers
- Primary DI / UDI-DI
- D678734701 FDA UDI
- FDA Product Code
- IWZ FDA UDI
- GMDN Term
- Digital imaging cassette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1840 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Digital imaging cassette
Plate Transfer Box by Air Techniques, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Digital imaging cassette.
- CR HD5.0 AEC CASSETTE — Agfa Corp. · Class II
- REGIUS Cassette — Konica Minolta, Inc. · Class II
- CR HD5.0 FLFS CASSETTE — Agfa Corp. · Class II
- CR MD4.0 GENERAL CASSETTE — Agfa Corp. · Class II
- CR MD4.0T GENERAL CASSETTE — Agfa Corp. · Class II
- CARESTREAM CR Cassette — CARESTREAM HEALTH, INC. · Class I
- CR MD4.0T GENERAL CASSETTE — Agfa Corp. · Class II
- CR HD5.0S GENERAL CASSETTE — Agfa Corp. · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Air Techniques, Inc.
Sources (1)
- FDA UDI ff2edd7c-f1fe-4aa5-ac99-64d538c77ba0 34 fields · synced Jun 9, 2026