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Replacement Finger Probes

FDA UDI

Class II (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name
Replacement Finger Probes FDA UDI
Generic Name
Pulse oximeter probe, reusable FDA UDI
Device Name
BCI 9 PIN REPLACEMENT FINGER PROBE FDA UDI
Model / Reference
20230 FDA UDI
Description
BCI 9 PIN REPLACEMENT FINGER PROBE FDA UDI

Identifiers

Catalog Number
20230 FDA UDI
Primary DI / UDI-DI
05060488570339 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 1 Inch FDA UDI
Length — 1 Inch FDA UDI
Width — 2 Inch FDA UDI

Category: Pulse oximeter probe, reusable

Replacement Finger Probes by Proactive Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Proactive Medical Products

Sources (1)

  • FDA UDI c74787cb-0237-404c-8093-e69e07367bb2 36 fields · synced Jun 1, 2026