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Polyp Traps

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MD-A-PT40Ref MD-A-PT25Ref MD-B-PT06Ref MD-B-PT04Ref MD-A-PT60

by Zhejiang Chuangxiang Medical Technology Co., LTD.

Identity

Trade Name
Polyp Traps EUDAMED
Polyp Trap FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Polyp Traps EUDAMED
Non-sterile FDA UDI
Model / Reference
MD-A-PT40 EUDAMEDFDA UDI
MD-A-PT25 EUDAMED
MD-B-PT06 EUDAMED
MD-B-PT04 EUDAMED
MD-A-PT60 EUDAMED
Description
Non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
06970401812202 EUDAMEDFDA UDI
06970401812196 EUDAMED
06970401812295 EUDAMED
06970401815593 EUDAMED
06970401812233 EUDAMED
Basic UDI-DI
697040181polyptrapTK EUDAMED
FDA Product Code
KDQ FDA UDI
EMDN Code
G030899 INSTRUMENTS FOR GASTRO-INTESTINAL ENDOSCOPY AND ECO-ENDOSCOPY, SINGLE-USE - OTHER EUDAMED
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue morcellation system handpiece, line-powered

Polyp Traps by Zhejiang Chuangxiang Medical Technology Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system handpiece, line-powered.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000012417
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (6)

  • EUDAMED a5ee8eac-4608-48bb-a292-65a2f78e3e29 61 fields · synced Jul 17, 2026
  • EUDAMED 05b55993-b9d4-4906-96a1-612c3339d434 61 fields · synced May 18, 2026
  • EUDAMED f84319f9-7c01-4185-800b-0d3428a48899 61 fields · synced May 18, 2026
  • EUDAMED 4d62b20b-7162-4f9b-8585-5863b21a365e 61 fields · synced May 18, 2026
  • EUDAMED b8cd9dc0-2d27-4e06-9567-402ead6e7920 61 fields · synced May 18, 2026
  • FDA UDI 95ec5c15-56a0-4dcf-bcc3-2670fd674eeb 33 fields · synced May 29, 2026