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SFI-Bar®

FDA UDI

Class II (US FDA UDI)

by Cendres+Métaux SA

Identity

Trade Name
SFI-Bar® FDA UDI
Generic Name
Bar dental precision attachment FDA UDI
Model / Reference
05000344 FDA UDI

Identifiers

Catalog Number
05000344 FDA UDI
Primary DI / UDI-DI
07640166510079 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Bar dental precision attachment FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

No

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
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI

Category: Bar dental precision attachment

SFI-Bar® by Cendres+Métaux SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bar dental precision attachment.

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 fb287095-381b-4d70-948a-5ffee8897392 35 fields · synced Jun 1, 2026