Identity
- Trade Name
- BMT Template Grid, Vertical Lock, Large FDA UDI
- Generic Name
- Manual brachytherapy system FDA UDI
- Model / Reference
- AC-B30205 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003072738 FDA UDI
- FDA Product Code
- IWJ FDA UDI
- GMDN Term
- Manual brachytherapy system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.5650 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Manual brachytherapy system
BMT Template Grid, Vertical Lock, Large by Concure Oncology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual brachytherapy system.
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- Applicator Brachytherapy Kit — Eckert & Ziegler BEBIG GmbH
- CivaDerm — CivaTech Oncology Inc. · Class II
- Advantage I-125® — ISOAID, L.L.C. · Class II
- AnchorLoad Brachytherapy Kit — Eckert & Ziegler BEBIG GmbH
- VariLoad Brachytherapy Kit PD-103 — Eckert & Ziegler BEBIG GmbH
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
- Concure Oncology, Inc.
Sources (1)
- FDA UDI 921f4983-e5d8-46de-80a8-d1dbb88a1853 32 fields · synced May 30, 2026