- Role
- Country
- Date of registration
- Address
CN-MF-000016558G1 094490 0008 Rev. 00No 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.ELECTRODE SURGICAL INSTRUMENTS is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by VHMED (Nantong) Co., Ltd.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jan 31, 2026
B-06971254921325Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06971254921325
3 warnings recorded — scroll inside the panel to see all entries.
CW001CW009CW007Sterile
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 Poland; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Jan 1, 2018 | Dec 31, 2028 |
| Austria | Jan 1, 2018 | Dec 31, 2028 |
| Belgium | Jan 1, 2018 | Dec 31, 2028 |
| Bulgaria | Jan 1, 2018 | Dec 31, 2028 |
| Germany | Jan 1, 2018 | Dec 31, 2028 |
| EL | Jan 1, 2018 | Dec 31, 2028 |
| Spain | Jan 1, 2018 | Dec 31, 2028 |
| France | Jan 1, 2018 | Dec 31, 2028 |
| Hungary | Jan 1, 2018 | Dec 31, 2028 |
| Italy | Jan 1, 2018 | Dec 31, 2028 |
| Romania | Jan 1, 2018 | 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.
06971254921325Basic 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-06971254921325LS6026LUDI 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.
K0201010602LAPAROSCOPIC AND THORACOSCOPIC ELECTROSURGERY FORCEPS, SINGLE-USENo certificate specifically references this device's Basic UDI-DI.
B-06971254922636On the marketELECTRODE SURGICAL INSTRUMENTSB-06971254923398On the marketELECTRODE SURGICAL INSTRUMENTSB-06971254923473On the marketELECTRODE SURGICAL INSTRUMENTSB-06971254922773On the marketELECTRODE SURGICAL INSTRUMENTSB-06971254923329On the marketELECTRODE SURGICAL INSTRUMENTSB-06971254924333On the market