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3D Obturation Kit

FDA UDI

Class I (US FDA UDI)

by Nusmile, Ltd

Identity

Trade Name
3D Obturation Kit FDA UDI
Generic Name
Endodontic obturation system FDA UDI
Device Name
Z-UP System + Z-DOWN System FDA UDI
Model / Reference
63800012K FDA UDI
Description
Z-UP System + Z-DOWN System FDA UDI

Identifiers

Primary DI / UDI-DI
00810092938675 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic obturation system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endodontic obturation systemEndodontic obturation system generator

3D Obturation Kit by Nusmile, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic obturation system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nusmile, Ltd

Sources (1)

  • FDA UDI fb6a63ed-38bc-4109-9aab-af9c068d2019 34 fields · synced Jun 1, 2026