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ProTech UBAR

FDA UDI

Class II (US FDA UDI)

by Protech Professional Products, Inc.

Identity

Trade Name
ProTech UBAR FDA UDI
Generic Name
Denture reliner, elastic, short-term FDA UDI
Device Name
ProTech UBAR Kit Shade 506RR - 160 gram powder, 200 ml monomer and 14 ml bonding liner FDA UDI
Model / Reference
RUCV11AD FDA UDI
Description
ProTech UBAR Kit Shade 506RR - 160 gram powder, 200 ml monomer and 14 ml bonding liner FDA UDI

Identifiers

Catalog Number
RUCV11AD FDA UDI
Primary DI / UDI-DI
D814RUCV11AD1 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Denture reliner, elastic, short-term FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

ProTech UBAR by Protech Professional Products, Inc. — 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

Sources (1)

  • FDA UDI 18989673-33a0-47a6-9433-64fdf578af97 35 fields · synced May 30, 2026