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Ohio

FDA UDI

Class I (US FDA UDI)

by Ohio Medical LLC

Identity

Trade Name
Ohio FDA UDI
Generic Name
General-gas low pressure tubing, reusable FDA UDI
Device Name
1' HOSE ASMBLY US NIT DF*SF COND 1/4" FDA UDI
Model / Reference
HS-01UN-DFSFC4 FDA UDI
Description
1' HOSE ASMBLY US NIT DF*SF COND 1/4" FDA UDI

Identifiers

Catalog Number
HS-01UN-DFSFC4 FDA UDI
Primary DI / UDI-DI
00628101508593 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
General-gas low pressure tubing, reusable 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

No

FDA UDI

Category: General-gas low pressure tubing, reusable

Ohio by Ohio Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-gas low pressure tubing, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ohio Medical LLC

Sources (1)

  • FDA UDI 65cefa74-d041-4e55-aad1-e9b4aadb6b39 35 fields · synced Jun 8, 2026