eudamed_udi
Primary ID: 03701273800782
STIMCARE ARTHRO (UDI 03701273800782)
Manufactured by TORTEL INDUSTRIES
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STIMCARE ARTHRO - Primary ID 03701273800782
Device Regulatory Overview
The STIMCARE ARTHRO (Model/Catalog Number: STIMCARE ARTHRO) is a medical device manufactured by TORTEL INDUSTRIES. This product is indexed under FDA Product Code / Category Classification M9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- STIMCARE ARTHRO
- Product Code / EMDN
- M9001
- Device Name
- STIMCARE ARTHRO
- Database Sync Date
- 2026-08-09 18:14:33
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 STIMCARE ARTHRO?
The registered manufacturer of record for STIMCARE ARTHRO is TORTEL INDUSTRIES.
What is the Primary UDI-DI identifier for STIMCARE ARTHRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701273800782.
What classification code is assigned to this device?
This device is registered under product classification code M9001.
Similar Classification Devices (M9001)
Other Devices by TORTEL INDUSTRIES
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