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Rainbow Saliva Ejectors

FDA UDI

Class I (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name
Rainbow Saliva Ejectors FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Pack of 100 Saliva Ejectors in assorted colors; pink, blue, green, purple FDA UDI
Model / Reference
7158222 FDA UDI
Description
Pack of 100 Saliva Ejectors in assorted colors; pink, blue, green, purple FDA UDI

Identifiers

Catalog Number
7158222 FDA UDI
Primary DI / UDI-DI
00723896022252 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

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: Dental suction system cannula, single-use

Rainbow Saliva Ejectors by Practicon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Practicon, Inc.

Sources (1)

  • FDA UDI fb2a8e0e-9a2b-4a13-a53f-bf3515920fa4 34 fields · synced Jun 1, 2026