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Implant Cleaning Brush

FDA UDI

Class I (US FDA UDI)

by Surgident

Identity

Trade Name
IMPLANT CLEANING BRUSH FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Model / Reference
ICB-02 FDA UDI

Identifiers

Primary DI / UDI-DI
08800041037728 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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
Sterilization Method
Microwave Radiation FDA UDI

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Implant Cleaning Brush by Surgident — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgident

Sources (1)

  • FDA UDI 97445f56-8347-4943-9187-4e2c043386e1 32 fields · synced Jun 1, 2026