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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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HYBRID, External fixator — 9 UDI-DI variants, MDR

MD Atlas
ProSpon, spol. s r.o.

Data from EUDAMED, last updated May 30, 2026

HYBRID, External fixator

8592395HYBRIDBB

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: ProSpon, spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8592395HYBRIDBB
Device name: HYBRID, External fixator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: ProSpon, spol. s r.o.
SRN: CZ-MF-000019992
Country: Czechia
Email: prospon@prospon.cz
Phone: +420312247763

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KSM7XHGZKA5K60YS3KX1NP01

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Carbon circular frame 140mm08595565101450
Carbon circular frame 160mm08595565101399
Carbon circular frame 180mm08595565101368
Carbon circular frame 200mm08595565101375
Carbon circular frame 220mm08595565101382
K-wire fixation device08595565101405
Perpendicular pivot for clamping Ø608595565101443
Straight pivot for clamping Ø608595565101436
UNI-FIX- Hybrid adaptor clamp08595565101467