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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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MD Atlas
Tianck Medical Co., Ltd.

Data from EUDAMED, last updated Jun 11, 2026

Hemodialysis Catheter

B-06971162815938

1 reference

Class IIa

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

Device family identification

Device name: Hemodialysis Catheter
Basic UDI-DI: B-06971162815938
Device model: Double lumen 14F×20cm
Issuing agency: EUDAMED
Version date: May 22, 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: Tianck Medical Co., Ltd.
SRN: CN-MF-000007451
Country: China
Email: sales1@tianck.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.

F900201Temporary hemodialysis catheters and kits

References by status

Legacy certificates

Certificate number: HD 2139971-1
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: May 26, 2024

References

1 reference

Export results

Applied filters

basicUdiUlid01KS6V37WHWDHDH59P9T8E01Z7

Format

Summary

31 columns included

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
032038	`032038`	`06971162815938`	1	On the market