eudamed_udi
Primary ID: 08594072953767
PAN2.04 Závěs ramenního kloubu M (UDI 08594072953767)
Manufactured by PANOP CZ s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAN2.04 Závěs ramenního kloubu M - Primary ID 08594072953767
Device Regulatory Overview
The PAN2.04 Závěs ramenního kloubu M (Model/Catalog Number: PAN2.04 M) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification M030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PAN2.04 M
- Product Code / EMDN
- M030501
- Device Name
- Závěs ramenního kloubu
- Database Sync Date
- 2026-08-09 16:48:06
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 PAN2.04 Závěs ramenního kloubu M?
The registered manufacturer of record for PAN2.04 Závěs ramenního kloubu M is PANOP CZ s.r.o..
What is the Primary UDI-DI identifier for PAN2.04 Závěs ramenního kloubu M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072953767.
What classification code is assigned to this device?
This device is registered under product classification code M030501.
Similar Classification Devices (M030501)
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