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Pencil probe

FDA UDI

Class II (US FDA UDI)

by Koven Technology, Inc.

Identity

Trade Name
Pencil probe FDA UDI
Generic Name
Invasive vascular ultrasound system probe FDA UDI
Device Name
Reusable CW Doppler pencil probe, 10 MHz FDA UDI
Model / Reference
BP10M5S8A FDA UDI
Description
Reusable CW Doppler pencil probe, 10 MHz FDA UDI

Identifiers

Catalog Number
BP10M5S8A FDA UDI
Primary DI / UDI-DI
00894912002890 FDA UDI
510(k) Number
K934638 FDA UDI
FDA Product Code
JOP FDA UDI
GMDN Term
Invasive vascular ultrasound system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2880 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
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Invasive vascular ultrasound system probe

Pencil probe by Koven Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive vascular ultrasound system probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25268828-6801-4ad1-a622-537f3404517a 36 fields · synced Jun 9, 2026