Identity
- Trade Name
- ULTRASOUND GASTROSCOPE FDA UDI
- Generic Name
- Flexible ultrasound gastroduodenoscope FDA UDI
- Device Name
- RADIAL ULTRASOUND VIDEO GASTROSCOPE 2.4C (REFURBISHED) FDA UDI
- Model / Reference
- EG-3670URK FDA UDI
- Description
- RADIAL ULTRASOUND VIDEO GASTROSCOPE 2.4C (REFURBISHED) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04961333232550 FDA UDI
- 510(k) Number
- K130206 FDA UDI
- FDA Product Code
- ODG FDA UDI
- GMDN Term
- Flexible ultrasound gastroduodenoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Flexible ultrasound gastroduodenoscope
Ultrasound Gastroscope by PENTAX of America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible ultrasound gastroduodenoscope.
- EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE — Olympus Medical Systems Corporation · Class II
- FUJIFILM — FUJIFILM Corporation · Class II
- EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE — Olympus Medical Systems Corporation · Class II
- PENTAX Medical — HOYA CORPORATION · Class II
- ULTRASONIC GASTROVIDEOSCOPE — Olympus Medical Systems Corporation · Class II
- FUJIFILM — FUJIFILM Corporation · Class II
- FUJIFILM — FUJIFILM Corporation · Class II
- PENTAX Medical — HOYA CORPORATION · Class II
Cleared under the same submission
K130206 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- PENTAX of America, Inc.
Sources (1)
- FDA UDI c2845256-a988-4397-98d4-fe7908efc701 34 fields · synced Jun 8, 2026