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Implant Remover

FDA UDI

Class I (US FDA UDI)

by Ebi, LLC

Identity

Trade Name
Implant Remover FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
IRFS FDA UDI

Identifiers

Primary DI / UDI-DI
08809476189941 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Dental implant system 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

No

FDA UDI

Implantable

Yes

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: Dental implant system

Implant Remover by Ebi, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ebi, LLC

Sources (1)

  • FDA UDI afaa6c07-5adb-4dd6-a77f-fe4bc6e7a2c1 32 fields · synced Jun 6, 2026