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Cath'N Sleeve Suction Kit

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Cath'N Sleeve Suction Kit FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
Cath'N Sleeve Suction Kit With Solution Container, CSR Wrap and Two Vinyl Gloves FDA UDI
Model / Reference
0089300 FDA UDI
Description
Cath'N Sleeve Suction Kit With Solution Container, CSR Wrap and Two Vinyl Gloves FDA UDI

Identifiers

Catalog Number
0089300 FDA UDI
Primary DI / UDI-DI
00801741050244 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
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 22 Inch FDA UDI
Catheter Gauge — 10 French FDA UDI

Cath'N Sleeve Suction Kit by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI ea594634-572d-4ff2-9e1e-6fd101bfa4c5 37 fields · synced May 31, 2026