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BeyesLube

FDA UDIEUDAMED

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
BeyesLUBE Aerosol Lubricant, For Turbines & Electric Handpieces, 500ml, Made in USA FDA UDI
Model / Reference
LC2010 FDA UDI
Description
BeyesLUBE Aerosol Lubricant, For Turbines & Electric Handpieces, 500ml, Made in USA FDA UDI

Identifiers

Primary DI / UDI-DI
00628504370384 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 — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument maintenance lubricant.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 86fdd449-27d3-4596-9b49-1b97265404bc 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026