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Davol Bronchial Aspirating Catheter

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Davol Bronchial Aspirating Catheter FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
Davol Suction Catheter X-Ray Opaque Rubber FDA UDI
Model / Reference
0109190 FDA UDI
Description
Davol Suction Catheter X-Ray Opaque Rubber FDA UDI

Identifiers

Catalog Number
0109190 FDA UDI
Primary DI / UDI-DI
00801741050565 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Davol Bronchial Aspirating Catheter 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 68e1c5ba-cacd-4a6c-95a5-347293c4d16b 37 fields · synced May 31, 2026