Identity
- Trade Name
- GEM IntraOp Doppler, Hand-Held Dopplers FDA UDI
- Generic Name
- Invasive/noninvasive vascular ultrasound probe FDA UDI
- Device Name
- Part Number 128770, Synovis Doppler Probe Sterile, 20 MHz, Box of 4 FDA UDI
- Model / Reference
- 128770 FDA UDI
- Description
- Part Number 128770, Synovis Doppler Probe Sterile, 20 MHz, Box of 4 FDA UDI
Identifiers
- Catalog Number
- 128770 FDA UDI
- Primary DI / UDI-DI
- 10817122020444 FDA UDI
- 510(k) Number
- K082870 FDA UDI
- FDA Product Code
- DPW FDA UDI
- GMDN Term
- Invasive/noninvasive vascular ultrasound probe FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Invasive/noninvasive vascular ultrasound probe
GEM IntraOp Doppler, Hand-Held Dopplers by Vascular Technology Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K082870 also covers:
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- Mizuho 07-150-10 Disposable Doppler Probe for Neurosurgery, Box — VASCULAR TECHNOLOGY INCORPORATED
- Mizuho 07-150-12 20 MHz Micro Disposable Doppler Probe, Box — VASCULAR TECHNOLOGY INCORPORATED
- Mizuho 07-150-21 20 MHz Disposable Doppler Probe Straight, Box — VASCULAR TECHNOLOGY INCORPORATED
- Mizuho 07-150-22 20 MHz Disposable Doppler Probe Curved Tip, Box — VASCULAR TECHNOLOGY INCORPORATED
- Mizuho 20 MHz Micro Disposable Doppler Probe, Box — VASCULAR TECHNOLOGY INCORPORATED
- Mizuho Power Supply Desktop 90-264 VAC — VASCULAR TECHNOLOGY INCORPORATED
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 |
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Manufacturer
- Manufacturer
- Vascular Technology Incorporated
Sources (1)
- FDA UDI f6b14a9a-38f3-46a1-a8fb-a5aa7920f37f 37 fields · synced May 30, 2026