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Adult Endotracheal Closed Suction System 24 Hours, Size 16f

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 16F FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 16F FDA UDI
Model / Reference
3240002 FDA UDI
Description
ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 16F FDA UDI

Identifiers

Primary DI / UDI-DI
05030267097814 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Airway suction catheter 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

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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Airway suction catheter

Adult Endotracheal Closed Suction System 24 Hours, Size 16f by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Airway suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 97d3cc57-b6ec-4de3-9402-b055225a287c 34 fields · synced Jun 8, 2026