PAN2.03 Ortéza ramenního kloubu-Gilchrist M (UDI 08594072953729)
Manufactured by PANOP CZ s.r.o.
Device Regulatory Overview
The PAN2.03 Ortéza ramenního kloubu-Gilchrist M (Model/Catalog Number: PAN2.03 M) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060621 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PAN2.03 M
- Product Code / EMDN
- Y060621
- Device Name
- Ortéza ramenního kloubu-Gilchrist
- Database Sync Date
- 2026-08-09 16:29:54
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 PAN2.03 Ortéza ramenního kloubu-Gilchrist M?
The registered manufacturer of record for PAN2.03 Ortéza ramenního kloubu-Gilchrist M is PANOP CZ s.r.o..
What is the Primary UDI-DI identifier for PAN2.03 Ortéza ramenního kloubu-Gilchrist M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072953729.
What classification code is assigned to this device?
This device is registered under product classification code Y060621.
Similar Classification Devices (Y060621)
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