Identity
- Trade Name
- Universal Cassette Holder FDA UDI
- Generic Name
- Radiation therapy port film device FDA UDI
- Model / Reference
- 11-335 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B365113350 FDA UDI
- FDA Product Code
- IXY FDA UDI
- GMDN Term
- Radiation therapy port film device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1880 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Radiation therapy port film device
Universal Cassette Holder by Aktina Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiation therapy port film device.
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 |
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Manufacturer
- Manufacturer
- Aktina Corp.
Sources (1)
- FDA UDI e44757e5-c258-4898-abf8-6054dacf9711 32 fields · synced Jun 8, 2026