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Medline Industries, Inc.

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
TRAY,CATHETER,SUCTION,6 FR,2 GLV,MINI FDA UDI
Model / Reference
DYND40986 FDA UDI
Description
TRAY,CATHETER,SUCTION,6 FR,2 GLV,MINI FDA UDI

Identifiers

Catalog Number
DYND40986 FDA UDI
Primary DI / UDI-DI
10080196997459 FDA UDI
FDA Product Code
OFR 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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI

Category: Airway suction catheter

Medline Industries, Inc. by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 1f270b62-e051-4543-aa63-a1b2f3468b4f 36 fields · synced Jun 1, 2026