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BeyesLube

FDA UDI

Class I (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
BeyesLube FDA UDI
Generic Name
Surgical instrument maintenance lubricant FDA UDI
Device Name
CareMaster Solution Plus for Automatic Machines, Synthetic,1000ml, Made in USA FDA UDI
Model / Reference
HPLP012 FDA UDI
Description
CareMaster Solution Plus for Automatic Machines, Synthetic,1000ml, Made in USA FDA UDI

Identifiers

Primary DI / UDI-DI
00628504370377 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Surgical instrument maintenance lubricant 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument maintenance lubricant

BeyesLube by Beyes Dental Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument maintenance lubricant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd79517c-49fa-48e1-8f04-0f25bbb45e0f 33 fields · synced May 30, 2026