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P.P SlimShaper ZS3

FDA UDI

Class I (US FDA UDI)

by Nusmile, Ltd

Identity

Trade Name
P.P SlimShaper ZS3 FDA UDI
Generic Name
Natural gutta-percha FDA UDI
Device Name
99 units FDA UDI
Model / Reference
PP-203 FDA UDI
Description
99 units FDA UDI

Identifiers

Primary DI / UDI-DI
00810118103599 FDA UDI
FDA Product Code
EKN FDA UDI
GMDN Term
Natural gutta-percha FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3830 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Natural gutta-percha

P.P SlimShaper ZS3 by Nusmile, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Natural gutta-percha.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nusmile, Ltd

Sources (1)

  • FDA UDI c56979dd-608a-4f9b-b9fc-274c011dd700 34 fields · synced Jun 6, 2026