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Bio-logic

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Bio-logic FDA UDI
Generic Name
Auditory stimulator FDA UDI
Device Name
ER2 replacement plastic tips for use with 580-ER2INS FDA UDI
Model / Reference
Insert Earphone Plastic Tip ER2 FDA UDI
Description
ER2 replacement plastic tips for use with 580-ER2INS FDA UDI

Identifiers

Catalog Number
202126 FDA UDI
Primary DI / UDI-DI
00382830052313 FDA UDI
510(k) Number
K031352 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Auditory stimulator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1050 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Auditory stimulator

Bio-logic by Natus Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Auditory stimulator.

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 d629fe54-5cd4-45a9-9589-4c7f8a44fa6f 36 fields · synced Jun 1, 2026