Rolled gauze, 7x150cm, 17-ply (UDI 08596222866286)
Manufactured by BATIST Medical Productions s.r.o.
Device Regulatory Overview
The Rolled gauze, 7x150cm, 17-ply (Model/Catalog Number: 1220130601) is a medical device manufactured by BATIST Medical Productions s.r.o.. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1220130601
- Product Code / EMDN
- M0201010102
- Device Name
- NESTERILNÍ GÁZOVÉ PRODUKTY / NON-STERILE GAUZE PRODUCTS
- Database Sync Date
- 2026-08-09 16:46:47
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 Rolled gauze, 7x150cm, 17-ply?
The registered manufacturer of record for Rolled gauze, 7x150cm, 17-ply is BATIST Medical Productions s.r.o..
What is the Primary UDI-DI identifier for Rolled gauze, 7x150cm, 17-ply?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08596222866286.
What classification code is assigned to this device?
This device is registered under product classification code M0201010102.
Similar Classification Devices (M0201010102)
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