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9013s0225

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name
9013S0225 FDA UDI
Generic Name
Analytical non-scalp cutaneous electrode FDA UDI
Device Name
9013S0225 Surface Electrodes FDA UDI
Model / Reference
70002-SC/AP/12 FDA UDI
Description
9013S0225 Surface Electrodes FDA UDI

Identifiers

Catalog Number
70002-SC/AP/12 FDA UDI
Primary DI / UDI-DI
05707480038213 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical non-scalp cutaneous electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI

Category: Analytical non-scalp cutaneous electrode

9013s0225 by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI b7b7f489-2476-4081-be6d-aa26e689868d 37 fields · synced Jun 1, 2026