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Tatum EZ Out Periotome

FDA UDI

Class I (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
Tatum EZ Out Periotome FDA UDI
Generic Name
Periotome, reusable FDA UDI
Device Name
Tatum EZ Out Periotome #2- for Atraumatic extraction of roots and teeth FDA UDI
Model / Reference
EZ Out Periotome #2 FDA UDI
Description
Tatum EZ Out Periotome #2- for Atraumatic extraction of roots and teeth FDA UDI

Identifiers

Catalog Number
EZ Out Periotome #2 FDA UDI
Primary DI / UDI-DI
00083208162008 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Periotome, reusable 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periotome, reusable

Tatum EZ Out Periotome by Suncoast Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periotome, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c96f34a2-3874-4a2b-a591-27121013adee 35 fields · synced May 30, 2026