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8000 Series Reusable Channel Cleaning Brush

FDA UDI

Class I (US FDA UDI)

by Primed Instruments Inc

Identity

Trade Name
8000 Series Reusable Channel Cleaning Brush FDA UDI
Generic Name
Endoscope cleaning brush, reusable FDA UDI
Device Name
Reusable Tapered Cleaning Brush. HIBC/UPN: M45381700 FDA UDI
Model / Reference
8170 FDA UDI
Description
Reusable Tapered Cleaning Brush. HIBC/UPN: M45381700 FDA UDI

Identifiers

Catalog Number
8170 FDA UDI
Primary DI / UDI-DI
00666416110049 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Endoscope cleaning brush, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope cleaning brush, reusable

8000 Series Reusable Channel Cleaning Brush by Primed Instruments Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope cleaning brush, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Primed Instruments Inc

Sources (1)

  • FDA UDI a0eb2871-3aad-4ac2-b874-06ef36fe3cab 37 fields · synced May 31, 2026