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Pepper Medical Closed Suction

FDA UDI

Class I (US FDA UDI)

by Pepper Medical, Inc.

Identity

Trade Name
Pepper Medical Closed Suction FDA UDI
Generic Name
Suction system catheter, general-purpose FDA UDI
Device Name
Closed Suction Catheter, 14 French FDA UDI
Model / Reference
CS24-DS-14 FDA UDI
Description
Closed Suction Catheter, 14 French FDA UDI

Identifiers

Catalog Number
CS24-DS-14 FDA UDI
Primary DI / UDI-DI
10850014575011 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Suction system catheter, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 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

No

FDA UDI

Over-the-Counter

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Suction system catheter, general-purpose

Pepper Medical Closed Suction by Pepper Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96f6db51-4b92-4e9c-b780-b086c23fcf9e 35 fields · synced May 30, 2026