Identity
- Trade Name
- Cs-137 Tube Source FDA UDI
- Generic Name
- Manual brachytherapy source, temporary placement FDA UDI
- Device Name
- Cs-137, 50 mCi, sealed source FDA UDI
- Model / Reference
- 67-6520 FDA UDI
- Description
- Cs-137, 50 mCi, sealed source FDA UDI
Identifiers
- Catalog Number
- 67-6520 FDA UDI
- Primary DI / UDI-DI
- 00858589006049 FDA UDI
- FDA Product Code
- KXK FDA UDI
- GMDN Term
- Manual brachytherapy source, temporary placement FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.5730 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Manual brachytherapy source, temporary placement
Cs-137 Tube Source by Eckert & Ziegler Isotope Products — 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
- Eckert & Ziegler Isotope Products
Sources (1)
- FDA UDI 913452b8-4b05-47b6-b841-97ad8bef3c55 34 fields · synced Jun 9, 2026