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QuickLine Primer 5ml bottle

FDA UDI

Class II (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name
QuickLine Primer 5ml bottle FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Light cure one-component surface coating material based on acrylates. FDA UDI
Model / Reference
220183 FDA UDI
Description
Light cure one-component surface coating material based on acrylates. FDA UDI

Identifiers

Primary DI / UDI-DI
00841549118487 FDA UDI
510(k) Number
K992609 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone dental impression material

QuickLine Primer 5ml bottle by Sterngold Dental LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d01a434-df5d-47bb-86b4-a5ccc1ec1e92 35 fields · synced May 30, 2026