MD Atlas
BlogPricingSign in
MD Atlas
Made In Tracker
Made In TrackerEasyUDI
Legal
Privacy PolicyLegal Notice
About
AboutFAQBlogPartnersContact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

  • MD Atlas
  • EPflex Feinwerktechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Guidewires for Central Circulatory Application

42556056gwcIIIEH

50 references

Class III
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class III
Manufacturer
EPflex Feinwerktechnik GmbH

Device family identification

Device name
Guidewires for Central Circulatory Application
Basic UDI-DI
42556056gwcIIIEH
Issuing agency
GS1
Version date
May 9, 2022

Classification

Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Risk category
Class III
Status
On the market

Manufacturer

Manufacturer

Name
EPflex Feinwerktechnik GmbH
SRN
DE-MF-000005425
Country
Germany
Email
ben.olwal@epflex.com

Device characteristics

No device characteristics flagged

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

  • C04010202Coronary artery therapeutic guidewires, non-hydrophilic
  • C0499Cardiovascular guidewires - other

References by status

Legacy certificates

Certificate number
1000265993
Type
refdata.certificate-mdr-type.quality-management-system
Notified body
DQS Medizinprodukte GmbH (0297)
Validity
Oct 27, 2025 → Nov 8, 2028
Certificate number
1000266008
Type
refdata.certificate-mdr-type.technical-documentation
Notified body
DQS Medizinprodukte GmbH (0297)
Validity
Oct 27, 2025 → Jul 2, 2029

References

50 references

Export results

Applied filters

  • basicUdiUlid·01G2C3XFQYCJVHDHXAXH5SZAF5

Format

Summary

31 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
  • Market country
  • Issuing entity
  • 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
  • DM Atlas link
Trade nameReference / catalog numberUDI-DI codeQuantityStatus
AMTMHFJ35220AMTMHFJ35220042556056072081On the market
AMTMHFJ35180AMTMHFJ35180042556056071851On the market
AMTMHFJD35150AMTMHFJD35150042556056070621On the market
4401350444013504042556056086631On the market
4501358245013582042556056082671On the market
TSX-035-270-35TSX-035-270-35042556056007801On the market
AMTMHFJD3570AMTMHFJD3570042556056071471On the market
AA-035-260-30AAA-035-260-30A042556056006811On the market
4501175645011756042556056003221On the market
AMTMHFJ35150AMTMHFJ35150042556056071611On the market
4301126743011267042556056001621On the market
4001306540013065042556056086011On the market
AMTMHFJ3570AMTMHFJ3570042556056071231On the market
TDS-035-270-25TDS-035-270-25042556056009401On the market
4801245048012450042556056004831On the market
TA-035-270-35TA-035-270-35042556056007041On the market
4901276849012768042556056016881On the market
4201074742010747042556056000631On the market
4001306640013066042556056086251On the market
AMTMHF38260AMTMHF38260042556056071091On the market
4501179345011793042556056003461On the market
AMTMHFJ35260BENAMTMHFJ35260BEN042556056070001On the market
4201331442013314042556056086491On the market
AMTMHF35150AMTMHF35150042556056070861On the market
AU-035-300-CAU-035-300-C042556056011831On the market