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Aria Valve Insert

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CA100-VIModel CA100-AK

by Cypress Adaptive LLC

Identity

Trade Name
Aria Valve Insert EUDAMED
Aria AK valve insert FDA UDI
Generic Name
External lower-limb prosthesis suspensory component, non-powered FDA UDI
Device Name
Aria Valve AK (above knee) EUDAMED
Aria AK Valve auto expulsion valve insert only FDA UDI
Model / Reference
CA100-AK EUDAMED
CA100-VI EUDAMEDFDA UDI
Description
Aria AK Valve auto expulsion valve insert only FDA UDI

Identifiers

Catalog Number
CA100-VI FDA UDI
Primary DI / UDI-DI
00850013242122 EUDAMEDFDA UDI
Basic UDI-DI
850013242VALVES74 EUDAMED
FDA Product Code
ISP FDA UDI
EMDN Code
Y99 DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - OTHER EUDAMED
GMDN Term
External lower-limb prosthesis suspensory component, non-powered FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.3420 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Aria Valve Insert by Cypress Adaptive, Llc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000016964
Authorised Representative
Romedis GmbH DE-AR-000037131

Sources (2)

  • EUDAMED d43fcd6e-6f9a-4f6e-b4f1-f75f4e014b1f 61 fields · synced Jul 25, 2026
  • FDA UDI 410531f8-54c2-4d20-90e3-caec4e4eb1ac 34 fields · synced May 29, 2026