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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
25' HOSE ASMB US AIR DF*DF COND 1/4" BRA FDA UDI
Model / Reference
HS-25UA-DFDFC4B FDA UDI
Description
25' HOSE ASMB US AIR DF*DF COND 1/4" BRA FDA UDI

Identifiers

Catalog Number
HS-25UA-DFDFC4B FDA UDI
Primary DI / UDI-DI
00628101588656 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 5a61b46f-43e5-4542-99a8-513a5deff08d 35 fields · synced May 30, 2026