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Precision Probe Tubes

FDA UDI

Class II (US FDA UDI)

by Precision Cast Plastic Parts, Inc.

Identity

Trade Name
Precision Probe Tubes FDA UDI
Generic Name
Audiometric/hearing aid tester FDA UDI
Device Name
Probe Tubes for Audiometric Testing FDA UDI
Model / Reference
U76MBY-40 FDA UDI
Description
Probe Tubes for Audiometric Testing FDA UDI

Identifiers

Catalog Number
U76MBY-40 FDA UDI
Primary DI / UDI-DI
00864994000343 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Audiometric/hearing aid tester 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

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

No

FDA UDI

Category: Audiometric/hearing aid tester

Precision Probe Tubes by Precision Cast Plastic Parts, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Audiometric/hearing aid tester.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 35fc6d2a-64db-4b8b-b7ff-5b9e1af6bff4 34 fields · synced May 30, 2026