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Resp-O2 Suction Catheter 14 FR Mini-Tray, Sterile

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Suction Catheter 14 FR Mini-Tray, Sterile FDA UDI
Generic Name
Secretion suction kit FDA UDI
Device Name
Contents: 1 One-Compartment Mini-Tray 1 Adult Graduated Catheter with Control Valve 1 Pair of Powder-Free Vinyl Gloves FDA UDI
Model / Reference
32083 FDA UDI
Description
Contents: 1 One-Compartment Mini-Tray 1 Adult Graduated Catheter with Control Valve 1 Pair of Powder-Free Vinyl Gloves FDA UDI

Identifiers

Primary DI / UDI-DI
00840117313514 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Secretion suction kit 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Secretion suction kit

Resp-O2 Suction Catheter 14 FR Mini-Tray, Sterile by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secretion suction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 86a7f2b6-24f0-4d7f-a582-d0c09a1c29d6 33 fields · synced Jun 8, 2026