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Axonics Accessory, Lead Stimulation Cable

EUDAMEDFDA UDI

Class AIMDD (EU MDR)

Ref 9007

by Axonics Inc.

Identity

Trade Name
Axonics Accessory, Lead Stimulation Cable EUDAMED
Axonics FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
Axonics Accessory, Lead Stimulation Cable EUDAMED
Tined Lead Test Stim. Cable FDA UDI
Model / Reference
9007 EUDAMEDFDA UDI
Description
Tined Lead Test Stim. Cable FDA UDI

Identifiers

Catalog Number
9007 FDA UDI
Primary DI / UDI-DI
10810005340257 EUDAMEDFDA UDI
Basic UDI-DI
B-10810005340257 EUDAMED
FDA Product Code
QON FDA UDI
EZW FDA UDI
EMDN Code
J020480 SACRAL SPINE IMPLANTABLE NEUROSTIMULATORS - ACCESSORIES EUDAMED
GMDN Term
Electrical-only medical device connection cable, single-use FDA UDI

Classification

Device Class
Class AIMDD EUDAMED
Class III FDA UDI
Regulation Number
876.5270 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Axonics Accessory, Lead Stimulation Cable by Axonics Inc. — Class AIMDD — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Axonics Inc.
EUDAMED SRN
US-MF-000008413
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED b2b5a63a-03be-4984-ab95-0a7f3209f0b6 61 fields · synced Jun 19, 2026
  • FDA UDI df9d968f-4696-4bfa-b3ad-fe8c79571b9a 35 fields · synced May 27, 2026