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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
Audiometric ear tip FDA UDI
Device Name
Insert Earphone Foam Tips, Jumbo FDA UDI
Model / Reference
Insert Earphone Tip Jumbo FDA UDI
Description
Insert Earphone Foam Tips, Jumbo FDA UDI

Identifiers

Catalog Number
202123 FDA UDI
Primary DI / UDI-DI
00382830052214 FDA UDI
510(k) Number
K031352 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Audiometric ear tip 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Audiometric ear tip

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

Similar devices

Also classified as Audiometric ear tip.

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 36f2f411-9407-4c07-88a6-b0f4cdf0d888 36 fields · synced May 31, 2026