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Compensatory Reserve Tablet T1 V2020.04.22

FDA UDI

Class II (US FDA UDI)

by Flashback Technologies, Inc.

Identity

Trade Name
Compensatory Reserve Tablet T1 V2020.04.22 FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Model / Reference
Compensatory Reserve Tablet T1 V2020.04.22 FDA UDI

Identifiers

Primary DI / UDI-DI
00860003025611 FDA UDI
FDA Product Code
PPW FDA UDI
GMDN Term
Pulse oximeter probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2200 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulse oximeter probe, single-use

Compensatory Reserve Tablet T1 V2020.04.22 by Flashback Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c4f836a7-aba9-44b3-a8ce-95009dd802ff 32 fields · synced Jun 1, 2026