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ROEKO Calcium Hydroxide PLUS Points

FDA UDI

Class II (US FDA UDI)

by Coltène/Whaledent AG

Identity

Trade Name
ROEKO Calcium Hydroxide PLUS Points FDA UDI
Generic Name
Root canal obturating point FDA UDI
Model / Reference
ISO 45 FDA UDI

Identifiers

Catalog Number
366845 FDA UDI
Primary DI / UDI-DI
E1653668451 FDA UDI
FDA Product Code
EJK FDA UDI
GMDN Term
Root canal obturating point FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3250 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

ROEKO Calcium Hydroxide PLUS Points by Coltène/Whaledent AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d96c1853-a1a0-4825-b1f9-ace1e8a01755 37 fields · synced May 31, 2026