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Brush

FDA UDI

Class U (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Brush FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Model / Reference
MH-362 FDA UDI

Identifiers

Primary DI / UDI-DI
04953170054358 FDA UDI
FDA Product Code
LFL FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI

Classification

Device Class
U 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

No

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: Surgical instrument/endoscope cleaning utensil, reusable

Brush by Olympus Medical Systems Corporation — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI e3289baa-dfde-49c7-886c-009fa06687db 33 fields · synced May 31, 2026