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Dry Tips

FDA UDI

Class I (US FDA UDI)

by Young Microbrush Llc

Identity

Trade Name
Dry Tips FDA UDI
Generic Name
Saliva absorbent FDA UDI
Device Name
Dry Tips Saliva Absorbent, X-Small FDA UDI
Model / Reference
292438 FDA UDI
Description
Dry Tips Saliva Absorbent, X-Small FDA UDI

Identifiers

Catalog Number
292438 FDA UDI
Primary DI / UDI-DI
00789594000992 FDA UDI
FDA Product Code
KHR FDA UDI
GMDN Term
Saliva absorbent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6050 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Saliva absorbent

Dry Tips by Young Microbrush Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Saliva absorbent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8ef63236-ea02-44f7-ac9c-1bd70105e685 35 fields · synced May 30, 2026