← Back to catalogue

Small nylon tubing

FDA UDI

Class I (US FDA UDI)

by Dreve Otoplastik GmbH

Identity

Trade Name
Small nylon tubing FDA UDI
Generic Name
Air-conduction hearing aid acoustic tube FDA UDI
Device Name
No. FDA UDI
Model / Reference
23010 FDA UDI
Description
No. FDA UDI

Identifiers

Catalog Number
23010 FDA UDI
Primary DI / UDI-DI
E239230101 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Air-conduction hearing aid acoustic tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3300 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Air-conduction hearing aid acoustic tube

Small nylon tubing by Dreve Otoplastik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid acoustic tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dreve Otoplastik GmbH

Sources (1)

  • FDA UDI 9d0582e1-edd8-4a2c-ab63-1b66b5e1aa64 36 fields · synced May 31, 2026