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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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OP02 — 56 UDI-DI variants, MDR (Borch Textile Group A/S)

MD Atlas
Borch Textile Group A/S

Data from EUDAMED, last updated May 23, 2026

OP02

5715765OP2H6

56 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: Borch Textile Group A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5715765OP2H6
Device name: OP02
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: Borch Textile Group A/S
SRN: DK-MF-000041570
Country: Denmark
Email: UMO@borchtextile.dk

Variants by status

UDI-DI variants

56 UDI-DI variants

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Applied filters

basicUdiUlid01J5X2YKHMZKQMRZ30QDQH156E

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

OP0205715765006499
OP0205715765006666
OP0205715765006703
OP0205715765007052
OP0205715765006505
OP0205715765006963

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