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Lw N° 4

FDA UDI

Class II (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
LW N° 4 FDA UDI
Generic Name
Dental brazing alloy FDA UDI
Device Name
LW N° 4 FDA UDI
Model / Reference
01050042_1PC FDA UDI
Description
LW N° 4 FDA UDI

Identifiers

Catalog Number
01050042 FDA UDI
Primary DI / UDI-DI
97640173080261 FDA UDI
FDA Product Code
EJT FDA UDI
GMDN Term
Dental brazing alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3060 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Lw N° 4 by Cendres+Métaux SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cendres+Métaux SA

Sources (1)

  • FDA UDI 34b2dda4-9de6-4eb4-b781-54c171675293 36 fields · synced May 31, 2026