- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Mar 30, 2026
B-06922798746202Disposable anal hemorrhoids ligation device is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Jiangsu Guanchuang Medical Technology Co., Ltd.. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000021127HD 2177655-1(01)06922798746202
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Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Denmark; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Mar 30, 2024 | Dec 31, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06922798746202Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-06922798746202GCTZB-2UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
H010201020102POLYAMIDE MULTIFILAMENT WITHOUT NEEDLEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →B-06922798748305On the marketDisposable anal hemorrhoids ligation deviceB-06922798746103On the marketDisposable anal hemorrhoids ligation deviceB-06922798747209On the marketDisposable anal hemorrhoids ligation deviceB-06922798746509On the marketDisposable anal hemorrhoids ligation deviceB-06922798748107On the marketDisposable anal hemorrhoids ligation deviceB-06922798747308On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
MDR.2292-2026/0051IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
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