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Endoscopic Video Image Processor
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
Ref RP-IPD-V2000BModel RP-IPD-V2000A, RP-IPD-V2000B, RP-IPD-V2000C, RP-IPD-V2000D
Identity
- Trade Name
- REDPINE FDA UDI
- Generic Name
- Endoscopic video image display unit FDA UDI
- Device Name
- Endoscopic Video Image Processor EUDAMED
- Model / Reference
- RP-IPD-V2000A, RP-IPD-V2000B, RP-IPD-V2000C, RP-IPD-V2000D EUDAMEDRP-IPD-V2000B EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 06972520301186 EUDAMEDFDA UDI
- Basic UDI-DI
- 697252030IPRO02GW EUDAMED
- 510(k) Number
- K232043 FDA UDI
- FDA Product Code
- FDF FDA UDIFDS FDA UDIFET FDA UDI
- EMDN Code
- Z12020406 VIDEO PROCESSORS EUDAMED
- GMDN Term
- Endoscopic video image display unit FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Endoscopic Video Image Processor by Guangzhou Red Pine Medical Instrument Co., Ltd. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K232043 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 697252030IPRO02GW | Class I | Active |
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Manufacturer
- Manufacturer
- Guangzhou Red Pine Medical Instrument Co., Ltd.
- EUDAMED SRN
- CN-MF-000012833
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (3)
- EUDAMED 1e6df4a6-8267-41e6-bc60-9d9fedcb2c9b 61 fields · synced Jul 13, 2026
- FDA UDI 567f8d92-a844-4128-b22e-e121554ad72c 33 fields · synced May 30, 2026
- FDA 510(k) K232043 1 fields · synced May 18, 2026