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Vivid Post Translucent

FDA UDI

Class I (US FDA UDI)

by Bioloren Srl

Identity

Trade Name
VIVID POST TRANSLUCENT FDA UDI
Generic Name
Pin/post dental drill bit FDA UDI
Device Name
Cylindrical fiberglass light transmitting posts kit (20 posts and 4 drills). FDA UDI
Model / Reference
B16-0050 FDA UDI
Description
Cylindrical fiberglass light transmitting posts kit (20 posts and 4 drills). FDA UDI

Identifiers

Primary DI / UDI-DI
08056099233111 FDA UDI
FDA Product Code
DZA FDA UDI
ELR FDA UDI
GMDN Term
Pin/post dental drill bit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
872.3810 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

No

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
Moist Heat or Steam Sterilization FDA UDI

Category: Root canal post, preformedPin/post dental drill bit

Vivid Post Translucent by Bioloren Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin/post dental drill bit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioloren Srl

Sources (1)

  • FDA UDI f97f7d54-c681-420a-9e2e-eb3f4914ff4d 33 fields · synced May 30, 2026