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Max-250tk

FDA UDI

Class II (US FDA UDI)

by Maxtec, Inc.

Identity

Trade Name
MAX-250TK FDA UDI
Generic Name
Respiratory oxygen sensor FDA UDI
Device Name
Oxygen Sensor W/ DC Connector FDA UDI
Model / Reference
R125P18-004 FDA UDI
Description
Oxygen Sensor W/ DC Connector FDA UDI

Identifiers

Primary DI / UDI-DI
00853061006623 FDA UDI
510(k) Number
K972992 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Respiratory oxygen sensor

Max-250tk by Maxtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory oxygen sensor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxtec, Inc.

Sources (1)

  • FDA UDI 0a759b60-1d4e-4000-bdb5-fe364b4353b4 34 fields · synced Jun 8, 2026