gudid
Primary ID: 1271-131
ARTHROSCOPIC TENDON KNIFE (UDI 1271-131)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARTHROSCOPIC TENDON KNIFE - Primary ID 1271-131
Device Regulatory Overview
The ARTHROSCOPIC TENDON KNIFE (Model/Catalog Number: 1271-131) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HTS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1271-131
- Product Code / EMDN
- HTS
- Device Name
- ARTHROSCOPIC TENDON KNIFE ROUND KNURL HANDLE
- Database Sync Date
- 2026-08-09 09:07:02
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ARTHROSCOPIC TENDON KNIFE?
The registered manufacturer of record for ARTHROSCOPIC TENDON KNIFE is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for ARTHROSCOPIC TENDON KNIFE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1271-131.
What classification code is assigned to this device?
This device is registered under product classification code HTS.
Similar Classification Devices (HTS)
Other Devices by SONTEC INSTRUMENTS, INC.
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