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Liqua Tip

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 006-00066Model 006-00065

by Cao Group, Inc.

Identity

Trade Name
Liqua-Tip EUDAMED
Liqua Tip FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
Liqua-Tip EUDAMED
Single-use luer-lock dental applicator brush. FDA UDI
Model / Reference
006-00065 EUDAMED
006-00066 EUDAMED
01807 FDA UDI
Description
Single-use luer-lock dental applicator brush. FDA UDI

Identifiers

Primary DI / UDI-DI
00872320000394 EUDAMED
00872320000455 EUDAMED
00872320004385 FDA UDI
Basic UDI-DI
87232000697PT EUDAMED
Unit of Use DI
00872320004385 EUDAMED
FDA Product Code
KXR FDA UDI
EMDN Code
Q010599 DENTAL INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3140 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 material application tool, single-use

Liqua Tip by Cao Group, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cao Group, Inc.

Sources (3)

  • FDA UDI 0f137e43-e876-43e6-9e9f-9233cb7ea24b 34 fields · synced Jul 12, 2026
  • EUDAMED 2cdeba16-6773-4d76-9682-7a28729ab2d6 61 fields · synced Jul 9, 2026
  • EUDAMED 5111ed92-5ed2-4bfd-bf97-e3b2cca52ec3 61 fields · synced Jul 12, 2026