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Aria safety barb O-ring

FDA UDI

Class I (US FDA UDI)

by Cypress Adaptive, Llc

Identity

Trade Name
Aria safety barb O-ring FDA UDI
Generic Name
External lower-limb prosthesis suspensory component, non-powered FDA UDI
Device Name
Spare parts/replacement parts for Aria valves FDA UDI
Model / Reference
CA300-O FDA UDI
Description
Spare parts/replacement parts for Aria valves FDA UDI

Identifiers

Catalog Number
CA300-O FDA UDI
Primary DI / UDI-DI
00850013242825 FDA UDI
FDA Product Code
ISP FDA UDI
GMDN Term
External lower-limb prosthesis suspensory component, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External lower-limb prosthesis suspensory component, non-powered

Aria safety barb O-ring by Cypress Adaptive, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External lower-limb prosthesis suspensory component, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cypress Adaptive, Llc

Sources (1)

  • FDA UDI d375c2e2-ad35-48ee-b59f-4c12b7f980fa 34 fields · synced May 30, 2026