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EUDAMED last updated this device on Mar 2, 2026
6903095TPER022J31401802 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Shandong Weigao Orthopaedic Device Company Limited.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0694208235983331401802(01)06942082359833
European Medical Device Nomenclature — the EU product classification assigned to this device.
L0927ORTHOPAEDIC SURGERY MANUAL PERFORATORS, REUSABLE1 warning recorded — scroll inside the panel to see all entries.
1.All instruments must be strictly sterilized before use. 2.The device belongs to class I device, and it is forbidden to implant into human body. 3.Reuse after sterilization. 4.During operation, it is forbidden to contact the unsterilized articles with the connections of the product. 5.The use of non-steroidal anti-inflammatory agents, anticoagulants and other biological factors will have adverse effects on the fusion. 6.Stop to use the device immediately in case of any deformation, bending, breaking, loosening, falling off, allergy etc. occurs. 7.Consumable products with cutting edge structures such as bone drill, guide pin, bone knife, etc. will gradually wear out during use. Before use, check the wear degree and replace it in time. 8.The device is only applicable for implants of Shandong Weigao Orthopaedic Device Co., Ltd. 9.The product must be used by trained professional doctors.
Primary placement in Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
CN-MF-000019785The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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 →Certificate health across this manufacturer's portfolio.
M.2025.MDR.1068AmendedM.2025.MDR.2024IssuedM.2026.MDR.1095IssuedNotified 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.
View in glossary →Notified 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.
View in glossary →Notified 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.
View in glossary →No certificate specifically references this device's Basic UDI-DI.