← Back to catalogue

Sage

FDA UDI

Class II (US FDA UDI)

by Sage Products Llc

Identity

Trade Name
Sage FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Suction Swab with Corinz FDA UDI
Model / Reference
6145 FDA UDI
Description
Suction Swab with Corinz FDA UDI

Identifiers

Catalog Number
6145 FDA UDI
Primary DI / UDI-DI
00618029821515 FDA UDI
FDA Product Code
JOL FDA UDI
NSB FDA UDI
KXF FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
872.6855 FDA UDI
880.6025 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Dental suction system cannula, single-useOral care kit, single-useDental tooth-cleaning solutionOral care swab

Sage by Sage Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral care swab.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sage Products Llc

Sources (1)

  • FDA UDI 7ee2b424-6c4e-447c-b003-d56ee9e25956 35 fields · synced Jun 8, 2026