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Visualase™ Neuro Accessories and Tools
EUDAMEDFDA UDIClass I (EU MDR)
Ref 9736541
by FHC Inc.
Identity
- Trade Name
- Visualase™ Neuro Accessories and Tools EUDAMEDVisualase Anchor Bolt Driver Guide FDA UDI
- Generic Name
- Neurological stereotactic surgery system FDA UDI
- Device Name
- Visualase Anchor Bolt Tools, Non-sterile EUDAMEDVisualase Anchor Bolt Guide for Leksell (1) Anchor Bolt Driver Guide for Leksell Coordinate Frame FDA UDI
- Model / Reference
- 9736541 EUDAMED9736541-00912 FDA UDI
- Description
- Visualase Anchor Bolt Guide for Leksell (1) Anchor Bolt Driver Guide for Leksell Coordinate Frame FDA UDI
Identifiers
- Catalog Number
- 9736541 FDA UDI
- Primary DI / UDI-DI
- 00873263009369 EUDAMED00873263009123 FDA UDI
- Basic UDI-DI
- 087326300.12-103-1-A.UL EUDAMED
- Direct Marketing DI
- 00873263009321 EUDAMED
- FDA Product Code
- HAO FDA UDI
- EMDN Code
- Z12100680 STEREOTACTIC NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Neurological stereotactic surgery system FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 882.4535 FDA UDI
- Market of Registration
- France 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Visualase™ Neuro Accessories and Tools by Fhc, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 087326300.12-103-1-A.UL | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- FHC Inc.
- EUDAMED SRN
- US-MF-000012111
- Authorised Representative
- TERMOBIT PROD SRL RO-AR-000010668
Sources (2)
- EUDAMED de662853-9260-4e5a-a47e-e75253d785be 61 fields · synced Jun 19, 2026
- FDA UDI 59709341-bcdc-4a54-b7fb-a28e2635a09b 35 fields · synced May 25, 2026