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EUDAMED last updated this device on Mar 27, 2026
692279870803MADisposable non-absorbable closure clips is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. 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.
16922798762049GCJZ-XL×5CN-MF-000021127(01)16922798762049
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
1. The closure clip cannot be used as an occlusion device for birth control of the oviduct tubes. 2. Closure clips cannot be used for ligation of renal arteries in nephrectomy for endoscopic donors. 3.Those who are allergic to the ingredients of this product and those with diffuse mucosal bleeding. 4.Those with cancerous ulcers who need hemostasis because of the fragile tissues at the lesions and the tissue clips are easy to fall off. 5.The hemostatic site needs to exceed the length of the clamp adapted to the tissue clamp, and the diameter of the blood vessel is too large to be suitable for patients with tissue clamp equipment. 6.Patients with advanced distant metastasis and immunosuppression or immunodeficiency of malignant tumors. 7.Patients with gastrointestinal ulcers and bleeding with severe tissue necrosis whose stump blood vessels are located in the center of the lesion and whose area is greater than 3cm2 have poor hemostasis due to tissue clips. Even if they are barely clamped, they are prone to relapse due to premature shedding.
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 | Oct 31, 2026 | Oct 31, 2029 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
H03030101SINGULAR NON-ABSORBABLE HAEMOSTASIS CLIPS FOR OPEN SURGERY AND VIDEOSURGERYPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →692279870803MAOn the marketDisposable non-absorbable closure clips692279870801M6On the marketDisposable non-absorbable closure clips692279870803MAOn the marketDisposable non-absorbable closure clips692279870802M8On the marketDisposable non-absorbable closure clips692279870803MAOn the marketDisposable non-absorbable closure clips692279870801M6On the marketNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.