Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Perpendicular pivot for clamping Ø6 — Class I MDR

MD Atlas
ProSpon, spol. s r.o.

EUDAMED last updated this device on May 27, 2026

Perpendicular pivot for clamping Ø6

8592395HYBRIDBB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ProSpon, spol. s r.o.
UDI-DI code: 08595565101443
Reference / catalog number: F0060109

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

Organization name: ProSpon, spol. s r.o.
SRN: CZ-MF-000019992
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: Perpendicular pivot for clamping Ø6
UDI-DI code: 08595565101443
Basic UDI-DI: 8592395HYBRIDBB
Reference / catalog number: F0060109
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: External fixator for the intended purpose of reposition, fixation and prolongation.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

P0912040101RADIAL BONE FIXATION SYSTEMS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas

Certificates

Certificate health across this manufacturer's portfolio.

2026-MDR/TD-003Issued
Technical documentationNotified body: 2265Expiry: Apr 26, 2029
2026-MDR/QS-003Issued
Quality management systemNotified body: 2265Expiry: Apr 26, 2029

Related devices

Carbon circular frame 140mm8592395HYBRIDBBOn the market Carbon circular frame 160mm8592395HYBRIDBBOn the market Carbon circular frame 180mm8592395HYBRIDBBOn the market Carbon circular frame 200mm8592395HYBRIDBBOn the market Carbon circular frame 220mm8592395HYBRIDBBOn the market