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Beesure

FDA UDI

Class I (US FDA UDI)

by Ascend Eagle Incorporated

Identity

Trade Name
Beesure FDA UDI
Generic Name
Denture repair kit, professional FDA UDI
Device Name
Beesure Micro Applicators 400 /BX , Black/White FDA UDI
Model / Reference
BE501D FDA UDI
Description
Beesure Micro Applicators 400 /BX , Black/White FDA UDI

Identifiers

Primary DI / UDI-DI
10817508021522 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Denture repair kit, professional FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Category: Denture repair kit, professional

Beesure by Ascend Eagle Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture repair kit, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48f19d9d-5dae-482f-a92c-33d00ae9aa74 34 fields · synced May 31, 2026