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Varian Universal Interstitial Cylinder Set
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref GM11013300
Identity
- Trade Name
- Varian Universal Interstitial Cylinder Set EUDAMEDFDA UDI
- Generic Name
- Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
- Device Name
- Varian Universal Interstitial Cylinder Set EUDAMEDContains: GM11013310-00816389027879, GM11013320-00816389027886, GM11013330-00816389027893, GM11013340-00816389027909 FDA UDI
- Model / Reference
- GM11013300 EUDAMEDFDA UDI
- Description
- Contains: GM11013310-00816389027879, GM11013320-00816389027886, GM11013330-00816389027893, GM11013340-00816389027909 FDA UDI
Identifiers
- Catalog Number
- GM11013300 FDA UDI
- Primary DI / UDI-DI
- 00816389027862 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00816389027862 EUDAMED
- 510(k) Number
- K193240 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
Yes
FDA UDI
Dry Heat Sterilization FDA UDI
MR Conditional FDA UDI
Varian Universal Interstitial Cylinder Set by Varian Medical Systems, Inc — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00816389027862 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Varian Medical Systems, Inc.
- EUDAMED SRN
- US-MF-000001784
- Authorised Representative
- Siemens Healthineers Nederland B.V. NL-AR-000000803
Sources (2)
- EUDAMED 0e2f148c-39fa-4a66-a462-9419be57a97a 61 fields · synced Jul 17, 2026
- FDA UDI a51de09b-c60c-4266-aafb-b85da43ac99d 35 fields · synced May 30, 2026