← Back to catalogue
kVue™ BoS™
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref RT-4535KV03Model Head and Neck
by Qfix
Identity
- Trade Name
- kVue™ BoS™ FDA UDI
- Generic Name
- Patient positioner base plate FDA UDI
- Device Name
- kVue BoS Couch Top Insert 24" Cantilever without Virtual Indexing FDA UDI
- Model / Reference
- RT-4535KV03 EUDAMEDFDA UDIHead and Neck EUDAMED
- Description
- kVue BoS Couch Top Insert 24" Cantilever without Virtual Indexing FDA UDI
Identifiers
- Catalog Number
- RT-4535KV03 FDA UDI
- Primary DI / UDI-DI
- 10841962108710 EUDAMEDFDA UDI
- Basic UDI-DI
- 8419621HEADNECKX4 EUDAMED
- FDA Product Code
- JAI FDA UDI
- EMDN Code
- Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
- GMDN Term
- Patient positioner base plate FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 892.5770 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
Yes
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
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 24 Inch FDA UDI
Category: Patient positioner base plate
kVue™ BoS™ by Qfix — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Patient positioner base plate.
- Meicen — Guangdong Meicen Medical Equipment Co., Ltd. · Class I
- Type-S™ Variable Axis Baseplate — Medtec LLC · Class II
- Posifix® -2 Baseplate — Medtec LLC · Class II
- MR Posi-S™ Adapter — Medtec LLC · Class II
- Uni-frame® Baseplate — Medtec LLC · Class II
- Prone Head Holder — Medtec LLC · Class I
- Arthrex TRIMANO quick adapter — Maquet, Inc. · Class I
- Uni-frame® Baseplate — Medtec LLC · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Qfix
Sources (2)
- FDA UDI 65b2ed87-507b-4e9f-bfc2-165488ff4186 36 fields · synced Jun 18, 2026
- EUDAMED 4dd87129-5395-4ed2-8f03-ad5ab2c6519e 61 fields · synced Jun 18, 2026