← Back to catalogue
Pair of titanium colpostat probes (left & right)
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref GM11010700
Identity
- Trade Name
- Pair of titanium colpostat probes (left & right) EUDAMEDFDA UDI
- Generic Name
- Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
- Device Name
- Titanium Fletcher-Style Applicator Set—Defined Geometry EUDAMEDFor Titanium Fletcher-style Applicator Set Defined Geometry FDA UDI
- Model / Reference
- GM11010700 EUDAMEDFDA UDI
- Description
- For Titanium Fletcher-style Applicator Set Defined Geometry FDA UDI
Identifiers
- Catalog Number
- GM11010700 FDA UDI
- Primary DI / UDI-DI
- 00810563022353 EUDAMEDFDA UDI00816389025561 FDA UDI
- Basic UDI-DI
- 089947500201059QB EUDAMED
- 510(k) Number
- K952913 FDA UDI
- FDA Product Code
- JAQ FDA UDI
- EMDN Code
- Z11010380 BRACHYTHERAPY RADIATION SYSTEMS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.5700 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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 UDIFDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Pair of titanium colpostat probes (left & right) by Varian Medical Systems, Inc — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 089947500201059QB | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Varian Medical Systems, Inc.
- EUDAMED SRN
- US-MF-000001784
- Authorised Representative
- Siemens Healthineers Nederland B.V. NL-AR-000000803
Sources (3)
- EUDAMED 6df9cc72-e46d-4edf-8261-8fc62739adc8 61 fields · synced Jun 18, 2026
- FDA UDI 9be95a57-49ac-4c44-b3af-04983e15b1f8 35 fields · synced May 30, 2026
- FDA UDI d9e8037e-b6a5-4d02-aacb-7b95e0ebd89a 34 fields · synced May 30, 2026