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Good Bi-Brush

FDA UDI

Class II (US FDA UDI)

by Hobbs Medical, Inc.

Identity

Trade Name
Good Bi-Brush FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI
Device Name
A device used to remove dirt or debris from the working channel(s) of the endoscope prior to disinfection and sterilization. It consists of a flexible insertion tube with plastic bristles. This is a single-use device. FDA UDI
Model / Reference
4665 FDA UDI
Description
A device used to remove dirt or debris from the working channel(s) of the endoscope prior to disinfection and sterilization. It consists of a flexible insertion tube with plastic bristles. This is a single-use device. FDA UDI

Identifiers

Catalog Number
4665 FDA UDI
Primary DI / UDI-DI
M84946653 FDA UDI
510(k) Number
K933354 FDA UDI
FDA Product Code
FEB FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical instrument/endoscope cleaning utensil, single-use

Good Bi-Brush by Hobbs Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hobbs Medical, Inc.

Sources (1)

  • FDA UDI 20cb8285-1379-4684-9df4-b61c39949f60 36 fields · synced May 30, 2026