← Back to catalogue

Parkell®

EUDAMEDFDA UDI

Class I (EU MDR)

Ref S496

by Parkell Inc.

Identity

Trade Name
Parkell® EUDAMEDFDA UDI
Generic Name
Dental material mixing nozzle FDA UDI
Device Name
Mixing Tip 3 EUDAMED
Mixing Tip with Aqua Base for MucoSoft®, MucoHard™, Sharp™ & Cinch™ (Pkg. of 30 pcs.) FDA UDI
Model / Reference
S496 EUDAMEDFDA UDI
Description
Mixing Tip with Aqua Base for MucoSoft®, MucoHard™, Sharp™ & Cinch™ (Pkg. of 30 pcs.) FDA UDI

Identifiers

Catalog Number
S496 FDA UDI
Primary DI / UDI-DI
10810000527011 EUDAMEDFDA UDI
Basic UDI-DI
081000052MIXINGTIP3JZ EUDAMED
Unit of Use DI
00810000527014 EUDAMED
FDA Product Code
ELW FDA UDI
EMDN Code
Q019006 DENTAL MATERIAL APPLICATION TIPS AND BRUSHES, SINGLE-USE EUDAMED
GMDN Term
Dental material mixing nozzle FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3660 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

No

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 injection cannula, single-use

Parkell® by Parkell, 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

Manufacturer
Parkell Inc.
EUDAMED SRN
US-MF-000003761
Authorised Representative
Directa AB SE-AR-000002492

Sources (2)

  • EUDAMED 21e932f1-7443-4da1-ac6c-18ae4e9b1946 61 fields · synced Jul 21, 2026
  • FDA UDI eb838409-c407-4951-8eeb-a6e0692640b4 35 fields · synced May 29, 2026