Ambu Subdermal CorkscrewSingle Patient Probes

FDA UDI

Class II (US FDA UDI)

by Ambu A/S

Identity

Trade Name: Ambu Subdermal CorkscrewSingle Patient Probes FDA UDI
Generic Name: Subdermal needle electrode FDA UDI
Device Name: Ambu IOM Corkscrew Needle 747 For EEG or EP monitoring during surgery. Disposable, with 6 lead wire colours (red, black, blue, yellow, white and green) Min. order is 24 pcs. = 1 box FDA UDI
Model / Reference: 74715-60/24 FDA UDI
Description: Ambu IOM Corkscrew Needle 747 For EEG or EP monitoring during surgery. Disposable, with 6 lead wire colours (red, black, blue, yellow, white and green) Min. order is 24 pcs. = 1 box FDA UDI

Identifiers

Catalog Number: 74715-60/24 FDA UDI
Primary DI / UDI-DI: 05707480107599 FDA UDI
FDA Product Code: GXZ FDA UDI
GMDN Term: Subdermal needle electrode FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 120 Centimeter FDA UDI
Length — 47 Inch FDA UDI
Lumen/Inner Diameter — 0.60 Millimeter FDA UDI

Category: Subdermal needle electrode

Ambu Subdermal CorkscrewSingle Patient Probes by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ambu A/S

Sources (1)

FDA UDI f07c3e9c-7fbc-4e8b-b604-48b5d486162d 37 fields · synced May 30, 2026