eudamed_udi
Primary ID: 04031815102111
NOBAKAWA® 21 x 38 CM (UDI 04031815102111)
Manufactured by NOBAMED Paul Danz AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOBAKAWA® 21 x 38 CM - Primary ID 04031815102111
Device Regulatory Overview
The NOBAKAWA® 21 x 38 CM (Model/Catalog Number: 102138) is a medical device manufactured by NOBAMED Paul Danz AG. This product is indexed under FDA Product Code / Category Classification M9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102138
- Product Code / EMDN
- M9001
- Device Name
- NOBAKAWA®
- Database Sync Date
- 2026-08-09 16:28:55
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 NOBAKAWA® 21 x 38 CM?
The registered manufacturer of record for NOBAKAWA® 21 x 38 CM is NOBAMED Paul Danz AG.
What is the Primary UDI-DI identifier for NOBAKAWA® 21 x 38 CM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031815102111.
What classification code is assigned to this device?
This device is registered under product classification code M9001.
Similar Classification Devices (M9001)
Other Devices by NOBAMED Paul Danz AG
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