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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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SRT Modified Holder Screwdriver… — 43 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

SRT Modified Holder Screwdriver Inserter Sleeve Clamp Template Reducer

0705034a001525U

43 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: Medos International SARL

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UDI-DI variants

43 UDI-DI variants

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basicUdiUlid01KH1M6YEJRX56TVX5SPFJMGG9

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

69710006110705034581354
69710011710705034605739
69710003610705034560984
69710008510705034581606
69710012610705034605838
69710012410705034606231
69710005910705034581750
69710006410705034581705
69710008610705034581682
69710007010705034581507
69710012910705034606194
69710005810705034581415
69710012510705034606262
69710012010705034606583
69710006010705034581774
69710008410705034581446
69710005610705034581729
69710012110705034606330
69710012310705034605968
69710006210705034581545
69710004710705034561011
69710005710705034581736
69710006710705034581385
69710011810705034606002
69710004510705034560908

1 2

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 0705034a001525U
Device name: SRT Modified Holder Screwdriver Inserter Sleeve Clamp Template Reducer
Device model: SRT Reusable Instruments for Insertion and Extraction
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medos International SARL
SRN: CH-MF-000014268
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 32 934 80 00

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status