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PRO3DURE SysTherm PU

FDA UDI

Class I (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
PRO3DURE SysTherm PU FDA UDI
Generic Name
Earmould, custom-made FDA UDI
Device Name
SysTherm PU pink-transparent standard packaging 2x50g FDA UDI
Model / Reference
SysTherm PU pink-transparent FDA UDI
Description
SysTherm PU pink-transparent standard packaging 2x50g FDA UDI

Identifiers

Catalog Number
A4020144 FDA UDI
Primary DI / UDI-DI
EPRCA4020144 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

PRO3DURE SysTherm PU 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

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Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI 851b2df2-17f8-41d0-ab1e-d1f5b3ab9445 35 fields · synced Jun 1, 2026