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
  • Shunmei Medical Co.,Ltd

Data from EUDAMED, last updated Jun 12, 2026

PTCA Guide Wire

B-06956014466216

1 reference

Class III
Applicable legislation
MDD [Directive 93/42/EEC on medical devices]
Risk category
Class III
Manufacturer
Shunmei Medical Co.,Ltd

Device family identification

Device name
PTCA Guide Wire
Basic UDI-DI
B-06956014466216
Issuing agency
EUDAMED
Version date
May 18, 2026

Classification

Applicable legislation
MDD [Directive 93/42/EEC on medical devices]
Risk category
Class III
Status
On the market

Manufacturer & authorised representative

Manufacturer

Name
Shunmei Medical Co.,Ltd
SRN
CN-MF-000001160
Country
China
Email
nora@shunmed.com

Authorised representative

Name
Lotus NL B.V.
SRN
NL-AR-000000121
Country
Netherlands
Phone
+31644168999

Device characteristics

No device characteristics flagged

EMDN code(s)

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

  • C04010101Coronary artery diagnostic guidewires, hydrophilic

References by status

Legacy certificates

Certificate number
CE-MDD-0017/02/2019/01
Type
refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body
Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi (2764)
Validity
Feb 6, 2024
Certificate number
CE-MDD-0017/02/2019/01/DD.03
Type
refdata.legacy.mdd-certificate-type.ii-4
Notified body
Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi (2764)
Validity
Feb 6, 2024

References

1 reference

Export results

Applied filters

  • basicUdiUlid·01KRXAREDWTE2CWR5TKA37KNR7

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
Shun P626621069560144662161On the market