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Dual Hose

FDA UDI

Class I (US FDA UDI)

by Maxtec, Inc.

Identity

Trade Name
Dual Hose FDA UDI
Generic Name
Medical air low pressure hose FDA UDI
Device Name
10' Air/Oxygen Blender Dual Hose with Ohmeda Wall Connector FDA UDI
Model / Reference
10' Air/Oxygen FDA UDI
Description
10' Air/Oxygen Blender Dual Hose with Ohmeda Wall Connector FDA UDI

Identifiers

Catalog Number
R129P17 FDA UDI
Primary DI / UDI-DI
00817770024361 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Medical air 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oxygen low pressure hoseMedical air low pressure hose

Dual Hose by Maxtec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical air low pressure hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxtec, Inc.

Sources (1)

  • FDA UDI fa8caf3a-f47a-4d92-b065-2e3ef50f42f7 34 fields · synced Jun 1, 2026