eudamed_udi
Primary ID: 06970557843822
Gauze Rolls (UDI 06970557843822)
Manufactured by Medwell Medical Products Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gauze Rolls - Primary ID 06970557843822
Device Regulatory Overview
The Gauze Rolls (Model/Catalog Number: R20021) is a medical device manufactured by Medwell Medical Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R20021
- Product Code / EMDN
- M0201010102
- Device Name
- Gauze Rolls
- Database Sync Date
- 2026-08-09 16:48:16
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 Gauze Rolls?
The registered manufacturer of record for Gauze Rolls is Medwell Medical Products Co., Ltd..
What is the Primary UDI-DI identifier for Gauze Rolls?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970557843822.
What classification code is assigned to this device?
This device is registered under product classification code M0201010102.
Similar Classification Devices (M0201010102)
Other Devices by Medwell Medical Products Co., Ltd.
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