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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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Instrument — 13 UDI-DI variants, MDR (BioComp Industries BV)

MD Atlas
BioComp Industries BV

Data from EUDAMED, last updated May 31, 2026

Instrument

87199799-INSTR-ORF-DR

13 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: BioComp Industries BV

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 87199799-INSTR-ORF-DR
Device name: —
Device model: Instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: BioComp Industries BV
SRN: NL-MF-000017324
Country: Netherlands
Email: info@biocomp.eu
Phone: +31736847200

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KSNSPWXE8947W2KGY783PE8M

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

BC-5000-65TZ3108719979904173
BC-5000-65RS0808719979902544
BC-5656-80RS2108719979903152
BC-5000-65TZ2708719979902582
BC-5000-65TZ2408719979902575
BC-5800-75RS7508719979903275
BC-5000-65RS1208719979902551
BC-5700-60RS8008719979903220
BC-5700-60RS7008719979903206
BC-5000-65RS1708719979902568
BC-50AS-65TZ2308719979904159
BC-5656-10RS7508719979903145
BC-5700-60RS1208719979903190