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O2-Sensor

FDA UDI

Class II (US FDA UDI)

by IT Dr. Gambert GmbH

Identity

Trade Name
O2-Sensor FDA UDI
Generic Name
Respiratory oxygen sensor FDA UDI
Model / Reference
M-12A FDA UDI

Identifiers

Catalog Number
410217 FDA UDI
Primary DI / UDI-DI
04250320600657 FDA UDI
FDA Product Code
CCL FDA UDI
GMDN Term
Respiratory oxygen sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1720 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Respiratory oxygen sensor

O2-Sensor by IT Dr. Gambert GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory oxygen sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
IT Dr. Gambert GmbH

Sources (1)

  • FDA UDI 66ab515f-6290-4424-bc50-69463180e02f 33 fields · synced Jun 8, 2026