VascuChek Clinical Probe

FDA UDI

Class II (US FDA UDI)

by Remington Medical, Inc.

Identity

Trade Name: VascuChek Clinical Probe FDA UDI
Generic Name: Laser Doppler blood flowmeter FDA UDI
Device Name: Clinical Probe (non-sterile) used with transceiver. FDA UDI
Model / Reference: VC-CP-01 FDA UDI
Description: Clinical Probe (non-sterile) used with transceiver. FDA UDI

Identifiers

Catalog Number: VC-CP-01 FDA UDI
Primary DI / UDI-DI: 00813079022657 FDA UDI
FDA Product Code: DPW FDA UDI
GMDN Term: Laser Doppler blood flowmeter 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 61.8 Millimeter FDA UDI

Category: Laser Doppler blood flowmeter

VascuChek Clinical Probe by Remington Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Remington Medical, Inc.

Sources (1)

FDA UDI f78ddfd6-4a7d-42d5-8a34-16da526e3b24 36 fields · synced Jun 8, 2026