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Alpine Biomed

FDA UDI

Class II (US FDA UDI)

by Alpine Biomed Aps

Identity

Trade Name
Alpine Biomed FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Device Name
HUSH Alligator Clip Cable, Shielded, 39", 5-pin DIN to red, black, green alligator clips FDA UDI
Model / Reference
9013C0232 FDA UDI
Description
HUSH Alligator Clip Cable, Shielded, 39", 5-pin DIN to red, black, green alligator clips FDA UDI

Identifiers

Primary DI / UDI-DI
05704736000970 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electromyographic needle electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Alpine Biomed by Alpine Biomed Aps — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alpine Biomed Aps

Sources (1)

  • FDA UDI 7d1d4ffc-3cd8-41c7-9e7f-18e31e0adee5 34 fields · synced Jun 7, 2026