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
  • SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.

Data from EUDAMED, last updated Jun 11, 2026

Dental Root-canal Instruments

B-06944835169300

1 reference

Class IIa
Applicable legislation
MDD [Directive 93/42/EEC on medical devices]
Risk category
Class IIa
Manufacturer
SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.

Device family identification

Device name
Dental Root-canal Instruments
Basic UDI-DI
B-06944835169300
Device model
X2
Issuing agency
EUDAMED
Version date
May 11, 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
SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.
SRN
CN-MF-000027059
Country
China
Email
martin.wang@supline.com
Phone
0086-755-26016156

Authorised representative

Name
Wellkang Ltd
SRN
XI-AR-000001836
Country
Northern Ireland
Phone
+44(78)58820000

Device characteristics

No device characteristics flagged

EMDN code(s)

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

  • Q010507Endodontic instruments (canal enlargers, files, rasps, etc.), single-use

References by status

Legacy certificates

Certificate number
DD601461680001
Type
refdata.legacy.mdd-certificate-type.v
Notified body
TÜV Rheinland LGA Products GmbH (0197)
Validity
Dec 31, 2028

References

1 reference

Export results

Applied filters

  • basicUdiUlid·01KRB0S5X787ADYFJFKV9T0J09

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
AB2600416BAB2600416B069448351693001On the market