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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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Safety Lancet — 19 UDI-DI variants, MDR (HTL-Strefa S.A.)

MD Atlas
HTL-Strefa S.A.

Data from EUDAMED, last updated May 31, 2026

Safety Lancet

590799609610MF

19 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: HTL-Strefa S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590799609610MF
Device name: Safety Lancet
Device model: Type 610
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: HTL-Strefa S.A.
SRN: PL-MF-000002198
Country: Poland
Email: justyna.zemigala@htl-strefa.pl
Phone: +48 664140189

Variants by status

UDI-DI variants

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KAGEV4DRG81A0YFJJ8F1AXYF

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

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681305903999607760
683705903999609320
683005903999609191
681205903999607746
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681605903999607791
682905903999609184
681505903999607784
922605903999608231
683105903999609269
680505903999608873
681705903999609160
683505903999609306
680405903999608866
922505903999608224
680305903999608859