← Back to catalogue

NaviTip Tips

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 4991

by Ultradent Products, Inc.

Identity

Trade Name
NaviTip Tips EUDAMED
NaviTip 29G Sideport FDA UDI
Generic Name
Dental material injection cannula, single-use FDA UDI
Device Name
Tips EUDAMED
NaviTips 29g 21mm Single Sideport 20pk (Yellow) FDA UDI
Model / Reference
4991 EUDAMEDFDA UDI
Description
NaviTips 29g 21mm Single Sideport 20pk (Yellow) FDA UDI

Identifiers

Catalog Number
4991 FDA UDI
Primary DI / UDI-DI
00883205033109 EUDAMEDFDA UDI
Basic UDI-DI
0883205-TF032AQ EUDAMED
FDA Product Code
EIC FDA UDI
EMDN Code
Q019006 DENTAL MATERIAL APPLICATION TIPS AND BRUSHES, SINGLE-USE EUDAMED
GMDN Term
Dental material injection cannula, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Germany 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

Yes

FDA UDI

Category: Dental material injection cannula, single-use

NaviTip Tips by Ultradent Products, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000013697
Authorised Representative
Ultradent Products GmbH DE-AR-000006666

Sources (2)

  • EUDAMED 9293838c-69e1-4046-8b14-079ce925b90d 61 fields · synced Jun 17, 2026
  • FDA UDI 679bfda7-53e8-4d3b-bd59-8d98b319f0d5 35 fields · synced May 30, 2026