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Ceri-Saw™

FDA UDI

Class I (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Ceri-Saw™ FDA UDI
Generic Name
Margin finishing dental file/rasp, reusable FDA UDI
Device Name
CERI-SAW ANTERIOR BLADES 10pc FDA UDI
Model / Reference
031336520 FDA UDI
Description
CERI-SAW ANTERIOR BLADES 10pc FDA UDI

Identifiers

Catalog Number
031336520 FDA UDI
Primary DI / UDI-DI
D8130313365201 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Margin finishing dental file/rasp, 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

Category: Margin finishing dental file/rasp, reusable

Ceri-Saw™ by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Margin finishing dental file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c911d5e-93ef-4860-935d-0aac7a245820 35 fields · synced Jun 9, 2026