Identity
- Trade Name
- MicroSelectron Digital FDA UDI
- Generic Name
- Brachytherapy system remote afterloading source transfer tube FDA UDI
- Device Name
- Coupling Treatment Tube for 4F Flexibles (8) FDA UDI
- Model / Reference
- 111508-00 FDA UDI
- Description
- Coupling Treatment Tube for 4F Flexibles (8) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08717213033412 FDA UDI
- FDA Product Code
- JAQ FDA UDI
- GMDN Term
- Brachytherapy system remote afterloading source transfer tube FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.5700 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Brachytherapy system remote afterloading source transfer tube
MicroSelectron Digital by Nucletron B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Brachytherapy system remote afterloading source transfer tube.
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- MicroSelectron Digital — Nucletron B.V. · Class II
- MicroSelectron Digital — Nucletron B.V. · Class II
- Flexitron — Nucletron B.V. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Nucletron B.V.
Sources (1)
- FDA UDI 045d1a60-7aa1-4c75-bca0-b967bbf568f3 35 fields · synced May 31, 2026