← Back to catalogue

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
NSG-BW FDA UDI

Identifiers

Catalog Number
1576700 FDA UDI
Primary DI / UDI-DI
04953170028533 FDA UDI
510(k) Number
K041566 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
Ethylene Oxide 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 53f92e0d-276a-428d-acb8-8be808b23b94 35 fields · synced Jun 1, 2026