eudamed_udi
Primary ID: 04035873011576
ARTHROSCOPE (UDI 04035873011576)
Manufactured by Henke-Sass, Wolf GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARTHROSCOPE - Primary ID 04035873011576
Device Regulatory Overview
The ARTHROSCOPE (Model/Catalog Number: 89550267) is a medical device manufactured by Henke-Sass, Wolf GmbH. This product is indexed under FDA Product Code / Category Classification Z12021101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 89550267
- Product Code / EMDN
- Z12021101
- Device Name
- Arthroscope
- Database Sync Date
- 2026-08-09 16:28:53
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 ARTHROSCOPE?
The registered manufacturer of record for ARTHROSCOPE is Henke-Sass, Wolf GmbH.
What is the Primary UDI-DI identifier for ARTHROSCOPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04035873011576.
What classification code is assigned to this device?
This device is registered under product classification code Z12021101.
Similar Classification Devices (Z12021101)
Other Devices by Henke-Sass, Wolf GmbH
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