← Back to catalogue

audioprint L-1 I MSI

FDA UDI

Class I (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
audioprint L-1 I MSI FDA UDI
Generic Name
Earmould, custom-made FDA UDI
Device Name
audioprint L-1 I MSI, 100 g; clear transparent FDA UDI
Model / Reference
100 g - Clear Transparent FDA UDI
Description
audioprint L-1 I MSI, 100 g; clear transparent FDA UDI

Identifiers

Catalog Number
A1040441 FDA UDI
Primary DI / UDI-DI
EPRCA1040441 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Earmould, custom-made 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Earmould, custom-made

audioprint L-1 I MSI by Pro3Dure Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earmould, custom-made.

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
Pro3Dure Medical

Sources (1)

  • FDA UDI 7a7e5365-035f-410e-9603-644aa4e14e5e 35 fields · synced May 31, 2026