← Back to catalogue

GEM IntraOp Doppler, Hand-Held Dopplers

FDA UDI

Class II (US FDA UDI)

by Vascular Technology Incorporated

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

Similar devices

Also classified as Invasive/noninvasive vascular ultrasound probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f6b14a9a-38f3-46a1-a8fb-a5aa7920f37f 37 fields · synced May 30, 2026