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rematitan®

FDA UDI

Class I (US FDA UDI)

by Dentaurum

Identity

Trade Name
rematitan® FDA UDI
Generic Name
Dental brazing alloy FDA UDI
Device Name
Pure titanium wire on coils, round, ø 0.4 mm, Length 2 m FDA UDI
Model / Reference
528-039-50 FDA UDI
Description
Pure titanium wire on coils, round, ø 0.4 mm, Length 2 m FDA UDI

Identifiers

Primary DI / UDI-DI
J011528039500 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Dental brazing alloy FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

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

No

FDA UDI

Category: Dental brazing alloy

rematitan® by Dentaurum — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental brazing alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentaurum

Sources (1)

  • FDA UDI a5f4b473-2ecd-40ae-9ec0-edd8ce9a9ce1 35 fields · synced Jun 8, 2026