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
  • Zhejiang Headway Medical Equipment Co., Ltd.

Data from EUDAMED, last updated Jun 13, 2026

Orthodontic Metal Brackets

B-06942721206672

1 reference

Class IIa
Applicable legislation
MDD [Directive 93/42/EEC on medical devices]
Risk category
Class IIa
Manufacturer
Zhejiang Headway Medical Equipment Co., Ltd.

Device family identification

Device name
Orthodontic Metal Brackets
Basic UDI-DI
B-06942721206672
Issuing agency
EUDAMED
Version date
Jun 10, 2026

Classification

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

Manufacturer & authorised representative

Manufacturer

Name
Zhejiang Headway Medical Equipment Co., Ltd.
SRN
CN-MF-000041591
Country
China
Email
sales@headwayortho.com

Authorised representative

Name
Luxus Lebenswelt GmbH
SRN
DE-AR-000005110
Country
Germany
Phone
+49 1715605732

Device characteristics

No device characteristics flagged

EMDN code(s)

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

  • Q010403Orthodontic brackets and buttons

References by status

Legacy certificates

Certificate number
DD 60131504 0001
Type
refdata.legacy.mdd-certificate-type.v
Notified body
TÜV Rheinland LGA Products GmbH (0197)
Validity
Aug 27, 2023

References

1 reference

Export results

Applied filters

  • basicUdiUlid·01KTQTP5JETMAKAEPVRXTHZ63B

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
H3151H3151069427212066721On the market