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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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SECUSORB — 3 UDI-DI variants, MDR (STS Medical Group AD)

MD Atlas
STS Medical Group AD

Data from EUDAMED, last updated May 23, 2026

SECUSORB

380023TD01TS0103TK

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: STS Medical Group AD

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 380023TD01TS0103TK
Device name: SECUSORB
Device model: ABDOMINAL SWABS WITH X-RAY, 45X45 CM, 6 PLIES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: STS Medical Group AD
SRN: BG-MF-000041809
Country: Bulgaria
Email: RegAffairs-STS@stsmedicalgroup.com
Phone: +359(0)74631554

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KM35FJMR9R6SGTH4WXF1KH1E

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

SECUSORB ABDOMINAL SWABS WITH X-RAY, 45X45 CM, 6 PLIES03800232423625
5253303800232424813
THORAXCOMPRESS-14PL 70X75/1 STERILE+RIBBONS03800232428194