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Hemorrhoidal Multi-Band Ligator with Anoscope

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref HM601-5BModel HM/601-5-B

by Changzhou Health Microport Medical Device Co., Ltd.

Identity

Trade Name
Hemorrhoidal Multi-Band Ligator with Anoscope EUDAMED
Hemorrhoidal Multi-Band Ligator with Anoscope FDA UDI
Generic Name
Haemorrhoid ligation set FDA UDI
Device Name
Hemorrhoidal Multi-Band Ligator with Anoscope EUDAMED
This product is used to treat the hemorrhoids in assistance of anoscope for adults only. FDA UDI
Model / Reference
HM/601-5-B EUDAMEDFDA UDI
HM601-5B EUDAMED
Description
This product is used to treat the hemorrhoids in assistance of anoscope for adults only. FDA UDI

Identifiers

Primary DI / UDI-DI
06951862291560 EUDAMEDFDA UDI
Basic UDI-DI
B-06951862291560 EUDAMED
FDA Product Code
FHN FDA UDI
EMDN Code
G020401 HAEMORRHOID LIGATURE SETS EUDAMED
GMDN Term
Haemorrhoid ligation set FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.4400 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

Yes

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Hemorrhoidal Multi-Band Ligator with Anoscope by Changzhou Health Microport Medical Device Co., Ltd — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000033536
Authorised Representative
Llins Service & Consulting GmbH DE-AR-000009077

Sources (2)

  • EUDAMED f4e55ab9-87bf-485f-8e93-741180c1eed7 61 fields · synced Jun 18, 2026
  • FDA UDI 7a9a96cb-ea10-489b-95f9-4d47df6f8a73 33 fields · synced May 26, 2026