← Back to catalogue

Impression Taking Refill Kit

FDA UDI

Class I (US FDA UDI)

by Westone Laboratories, Inc.

Identity

Trade Name
Impression Taking Refill Kit FDA UDI
Generic Name
Earmould impression material FDA UDI
Device Name
Impression Taking Refill Kit - Refill for Impression taking kit FDA UDI
Model / Reference
NA FDA UDI
Description
Impression Taking Refill Kit - Refill for Impression taking kit FDA UDI

Identifiers

Catalog Number
10162 FDA UDI
Primary DI / UDI-DI
00850047788474 FDA UDI
FDA Product Code
LDG FDA UDI
GMDN Term
Earmould impression material 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

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

Yes

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 impression material

Impression Taking Refill Kit by Westone Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earmould impression material.

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

Sources (1)

  • FDA UDI bf4ccf04-a716-4470-91a3-73400081fe29 34 fields · synced May 30, 2026