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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Flexible endoscopic cytology brush, single-use FDA UDI
Device Name
ConMed Disposable Bronchial Cytology Brush, 1 mm X 120 cm FDA UDI
Model / Reference
133 FDA UDI
Description
ConMed Disposable Bronchial Cytology Brush, 1 mm X 120 cm FDA UDI

Identifiers

Catalog Number
133 FDA UDI
Primary DI / UDI-DI
20845854082123 FDA UDI
FDA Product Code
FDX FDA UDI
GMDN Term
Flexible endoscopic cytology brush, 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

Yes

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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 120 Centimeter FDA UDI
Width — 1 Millimeter FDA UDI
Length — 11 Millimeter FDA UDI
Width — 1.7 Millimeter FDA UDI

Category: Flexible endoscopic cytology brush, single-use

Conmed by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic cytology brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 54f1ba6f-bb56-463d-ab03-f86e6d58372d 36 fields · synced Jun 8, 2026