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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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12-2 Fol.Stretcher — 2 UDI-DI variants, MDR (Bucher Leichtbau AG)

MD Atlas
Bucher Leichtbau AG

Data from EUDAMED, last updated May 23, 2026

12-2 Fol.Stretcher

7649989816STR-S0033C

2 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: Bucher Leichtbau AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649989816STR-S0033C
Device name: 12-2 Fol.Stretcher
Device model: 12-2 Fol.Stretcher
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Bucher Leichtbau AG
SRN: CH-MF-000017716
Country: Switzerland
Email: bucher@bucher-group.com
Phone: +41448062424

Authorised representative

Name: Bucher Interiors GmbH
SRN: DE-AR-000006455
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GK3ZAGWXWS3CMMVZ2D8WNXGR

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

12-2 FOL.STRETCHER07649989816047
CUSHION ASSY07649998867504