Identity
- Trade Name
- TAYLOR MICRO ARTHROSCOPIC PROBE FDA UDI
- Generic Name
- Stereotactic surgery system probe, reusable FDA UDI
- Device Name
- TAYLOR MICRO ARTHROSCOPIC PROBE FDA UDI
- Model / Reference
- 1271-120 FDA UDI
- Description
- TAYLOR MICRO ARTHROSCOPIC PROBE FDA UDI
Identifiers
- Catalog Number
- 1271-120 FDA UDI
- Primary DI / UDI-DI
- 00192896083998 FDA UDI
- FDA Product Code
- HXB FDA UDI
- GMDN Term
- Stereotactic surgery system probe, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 8 Inch FDA UDI
Category: Stereotactic surgery system probe, reusable
Taylor Micro Arthroscopic Probe by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Stereotactic surgery system probe, reusable.
- Head Pin 2.5x60mm, 10 pack w/o CE — MAZOR ROBOTICS LTD · Class II
- Rear Panel Adaptor — MAZOR ROBOTICS LTD · Class II
- SIES-Long Tapered Drill 3x80, 5 pack — MAZOR ROBOTICS LTD · Class II
- Renaissance Surgical Accessories Kit — MAZOR ROBOTICS LTD · Class II
- 5.5/6.0 Arm Guide Screw Kit — MAZOR ROBOTICS LTD · Class II
- SURGICAL_INSTRUMENTS, BED CONNECTOR — MAZOR ROBOTICS LTD · Class II
- SA 3.0mm Short Drill, 10 pack — MAZOR ROBOTICS LTD · Class II
- ACUFEX — Smith & Nephew, Inc. · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sontec Instruments, Inc.
Sources (1)
- FDA UDI efd6d714-d4fb-4e07-8838-daa067ac4321 36 fields · synced Jun 6, 2026