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Procodile

FDA UDI

Class I (US FDA UDI)

by Sure Dent Corporation

Identity

Trade Name
Procodile FDA UDI
Generic Name
Endodontic paper point FDA UDI
Device Name
Absorbent Paper Points Taper .06,.05, Size 25-30,35-40, 60/PK, mm marked, SB, 25-30/.06,35-40/.05 FDA UDI
Model / Reference
PPPR06 FDA UDI
Description
Absorbent Paper Points Taper .06,.05, Size 25-30,35-40, 60/PK, mm marked, SB, 25-30/.06,35-40/.05 FDA UDI

Identifiers

Primary DI / UDI-DI
18809264297800 FDA UDI
FDA Product Code
EKN FDA UDI
GMDN Term
Endodontic paper point 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endodontic paper point

Procodile by Sure Dent Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic paper point.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d86aea9f-b11e-4707-9380-0a5da0de1f61 34 fields · synced May 30, 2026