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Stimulator Box

FDA UDI

Class III (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name
Stimulator Box FDA UDI
Generic Name
Nerve location/function operative test pulse generator FDA UDI
Device Name
Hardware Interface System FDA UDI
Model / Reference
37005 FDA UDI
Description
Hardware Interface System FDA UDI

Identifiers

Primary DI / UDI-DI
09008737370053 FDA UDI
PMA Number
P000025 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Nerve location/function operative test pulse generator FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Nerve location/function operative test pulse generator

Stimulator Box by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9478458e-a344-4743-8fb6-6a43eb340d0e 34 fields · synced Jun 8, 2026