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O-Two

FDA UDI

Class I (US FDA UDI)

by O-Two Medical Technologies Inc

Identity

Trade Name
O-Two FDA UDI
Generic Name
Oxygen low pressure hose FDA UDI
Device Name
Supply Hose Assembly FDA UDI
Model / Reference
17MP1329 FDA UDI
Description
Supply Hose Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
07540195015029 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Oxygen low pressure hose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oxygen low pressure hose

O-Two by O-Two Medical Technologies Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen low pressure hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
O-Two Medical Technologies Inc

Sources (1)

  • FDA UDI 1168d7fe-adc2-475a-accb-3a3624d16690 34 fields · synced May 30, 2026