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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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Traumastem — 154 UDI-DI variants, MDR (BIOSTER, a.s.)

MD Atlas
BIOSTER, a.s.

Data from EUDAMED, last updated May 23, 2026

Traumastem

85903170010SG

154 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: BIOSTER, a.s.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 24 0146 TD/NB
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390 (1023)
Validity: Apr 29, 2024 → Apr 28, 2029

Identity & classification

Basic UDI-DI: 85903170010SG
Device name: Traumastem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: May 7, 2024

Manufacturer & authorised representative

Manufacturer

Name: BIOSTER, a.s.
SRN: CZ-MF-000011615
Country: Czechia
Email: bioster@bioster.cz
Phone: +420 549 429 111

Variants by status

UDI-DI variants

154 UDI-DI variants

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Applied filters

basicUdiUlid01HX8YJQEFDQAYHF2EMKCEHNT3

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

1020818590317102089
1021118590317102119
1022728590317102277
1005718590317100573

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