LineGene 9600 Plus Fluorescent Quantitative Detection System
EUDAMEDFDA UDIClass A (EU MDR)
Identity
- Trade Name
- LineGene 9600 Plus Fluorescent Quantitative Detection System EUDAMEDBIOER LineGene 9600 Plus Fluorescent Quantitative Detection System FDA UDI
- Generic Name
- Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
- Device Name
- LineGene 9600 Plus Fluorescent Quantitative Detection System EUDAMEDFor the detail information, please refer to the IFU. FDA UDI
- Model / Reference
- FQD-96A(EA2), FQD-96A(EA4), FQD-96A(EA5), FQD-96A(EA6) EUDAMEDFQD-96A(EA4) EUDAMEDFDA UDI
- Description
- For the detail information, please refer to the IFU. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06973843220772 EUDAMED06973843220536 FDA UDI
- Basic UDI-DI
- 697384322FQD004GW EUDAMED
- Direct Marketing DI
- 06973843220772 EUDAMED
- FDA Product Code
- OOI FDA UDI
- EMDN Code
- W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED
- GMDN Term
- Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass II FDA UDI
- Regulation Number
- 862.2570 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Contains Latex
No
Human Tissues
No
Animal Tissues
No
Microbial Substances
No
Reagent
No
Self Testing
No
Near-Patient Testing
No
Professional Testing
Yes
Companion Diagnostics
No
Surgical Instrument
Yes
New Device
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
Yes
Category: Nucleic acid sample preparation instrument IVD
LineGene 9600 Plus Fluorescent Quantitative Detection System by Hangzhou Bioer Technology Co., Ltd. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/IVDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 697384322FQD004GW | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Hangzhou Bioer Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000019512
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (2)
- EUDAMED 95aca892-4239-40a0-8084-49ab9f382646 61 fields · synced Jun 8, 2026
- FDA UDI 2798c0b7-619c-41b5-ab65-c8fb8c903724 33 fields · synced May 30, 2026