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Single-use Flexible Cystoscope

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref CY-E2G01

by Hunan Vathin Medical Instrument Co., Ltd.

Identity

Trade Name
Single-Use Flexible Cystoscope FDA UDI
Generic Name
Flexible video cystoscope, single-use FDA UDI
Device Name
Single-use Flexible Cystoscope EUDAMED
Model / Reference
CY-E2G01 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06972197483888 EUDAMED
06972197482423 FDA UDI
Basic UDI-DI
697219748CY4E EUDAMED
510(k) Number
K242535 FDA UDI
FDA Product Code
FAJ FDA UDI
EMDN Code
Z12020701 CYSTOSCOPES EUDAMED
GMDN Term
Flexible video cystoscope, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Single-use Flexible Cystoscope by Hunan Vathin Medical Instrument Co., Ltd. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000002593
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (3)

  • EUDAMED c3dda6d5-b8d5-45d8-a661-972d4d1ec02a 61 fields · synced Sep 18, 2026
  • FDA UDI d05e37e7-7d6d-4ce3-ae19-11acd169cf27 33 fields · synced May 29, 2026
  • FDA 510(k) K221580 1 fields · synced May 18, 2026