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Grason-Stadler

FDA UDI

Class II (US FDA UDI)

by Diagnostic Group Llc

Identity

Trade Name
Grason-Stadler FDA UDI
Generic Name
Vestibulo-auditory analysis system FDA UDI
Model / Reference
GSI Audera Pro FDA UDI

Identifiers

Primary DI / UDI-DI
00810046700495 FDA UDI
FDA Product Code
GWJ FDA UDI
GMDN Term
Vestibulo-auditory analysis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1900 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

Yes

FDA UDI

Category: Vestibulo-auditory analysis system

Grason-Stadler by Diagnostic Group Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vestibulo-auditory analysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4dd58401-0ed6-434c-8a0d-d3e07a234ca0 32 fields · synced May 30, 2026