← Back to catalogue
Single-Use Video Gastroscope
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref RP-GI-G02BModel RP-GI-G02A, RP-GI-G02B
Identity
- Trade Name
- Single-Use Video Gastroscope EUDAMEDREDPINE FDA UDI
- Generic Name
- Flexible video gastroscope, single-use FDA UDI
- Device Name
- Single-Use Video Gastroscope EUDAMED
- Model / Reference
- RP-GI-G02A, RP-GI-G02B EUDAMEDRP-GI-G02B EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 06972520301100 EUDAMEDFDA UDI
- Basic UDI-DI
- 697252030GASF019P EUDAMED
- 510(k) Number
- K232043 FDA UDI
- FDA Product Code
- FDF FDA UDIFDS FDA UDIFET FDA UDI
- EMDN Code
- Z12020506 GASTROSCOPES EUDAMED
- GMDN Term
- Flexible video gastroscope, single-use FDA UDI
Classification
- Device Class
- Class IIa 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
Yes
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
Single-Use Video Gastroscope by Guangzhou Red Pine Medical Instrument Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 697252030GASF019P | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
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 (2)
- EUDAMED 34c111d4-85d6-42ce-855b-b4cd995b390b 61 fields · synced Jul 12, 2026
- FDA UDI aa5e3c20-b8c4-41d8-8ad2-680a4df4f211 33 fields · synced May 30, 2026