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Vitalcontrol

FDA UDI

Class II (US FDA UDI)

by Beurer North America, L.p.

Identity

Trade Name
Vitalcontrol FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
SPO25 Pulse Oximeter EAN 4066299453886 Art. No 453.88 FDA UDI
Model / Reference
SPO25 FDA UDI
Description
SPO25 Pulse Oximeter EAN 4066299453886 Art. No 453.88 FDA UDI

Identifiers

Primary DI / UDI-DI
00850018808088 FDA UDI
FDA Product Code
PGJ FDA UDI
GMDN Term
Pulse oximeter 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulse oximeter

Vitalcontrol by Beurer North America, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 817e55ca-5df8-4c96-8982-3c5d0490cfe5 34 fields · synced May 30, 2026