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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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Extensions / Couplings — 5 UDI-DI variants, MDR (PB Swiss Tools AG)

MD Atlas
PB Swiss Tools AG

Data from EUDAMED, last updated May 23, 2026

Extensions / Couplings

7610733MD47847CR

5 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: PB Swiss Tools AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7610733MD47847CR
Device name: Extensions / Couplings
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: PB Swiss Tools AG
SRN: CH-MF-000040741
Country: Switzerland
Email: regulatory@pbswisstools.com
Phone: +41344377171

Authorised representative

Name: MDSS GmbH
SRN: DE-AR-000005430
Country: Germany

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KKXJQ270QK7AKT8KCB2G4S2B

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

8000807610733800087
8001007610733800100
8000707610733800070
8001107610733800117
8000607610733800063