FDA.reportPublic FDA data

Bard Button Device Bolus Device Bolus Feeding Tube with Straight Adaptor

Primary DI
10801741080835
Brand
Bard Button Device Bolus Device Bolus Feeding Tube with Straight Adaptor
Company
Bard Access Systems, Inc.
Model
000257
Catalog number
000257
Device description
Bolus Tube for 18 Fr
Published
2015-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KGCTUBE, GASTRO-ENTEROSTOMY

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KGCTube, Gastro-EnterostomyGastroenterology, Urology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10801741080835PackageGS117Not in Commercial Distribution
20801741080832PackageGS112In Commercial Distribution
00801741080838PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1080174108083510801741080835
2080174108083220801741080832
00801741080838008017410808388017410808380801741080838

GMDN Terms#

Term, Definition table
TermDefinition
Gastrostomy tubeA thin, flexible, hollow tube intended to be percutaneously inserted into the stomach, typically through puncture of the abdominal wall and stomach after distention of the stomach by endoscopic methods. It is intended to feed a patient with a physical disability that prevents oral feeding (e.g., a birth defect of the stomach), and/or provide drainage/decompression of the stomach when it is necessary to bypass an obstruction of the stomach outlet into the small intestine. Additional disposable enteral feeding components (e.g., external tubing, syringe) may be included. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Catheter Gauge18French
Length61Centimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)545-0890medical.services@crbard.com

Regulatory Flags#

DUNS number
044611812
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00801741036712Groshong771070077107002015-09-24
00801741036729Groshong771155077115502015-09-24
00801741037696Groshong772495077249502015-09-24
00801741037719Groshong774155077415502015-09-24
10801741239356PowerPICC Sherlock 3CGCK001067ACK001067A2026-03-11
10801741239363PowerPICC ProvenaCK001068ACK001068A2026-03-11
10801741239370PowerPICC ProvenaCK001069ACK001069A2026-03-11
10801741239271MiniLocCPA00072CPA000722026-02-26
10801741238830PowerPICC Provena SOLOCK001091CK0010912026-02-11
00801741038464Niagara Slim-Cath catheter543215054321502015-12-04
00801741038471Niagara Slim-Cath Catheter543220054322002015-11-20
00801741038488Niagara Slim-Cath catheter543224054322402015-12-04
00801741045141Niagara Slim-Cath catheter543412054341202015-11-20
00801741045158Niagara Slim-Cath catheter543415054341502015-11-06
10801741231275CentroVena One1K0R72161K0R72162026-01-23
10801741231282CentroVena One1K0R72201K0R72202026-01-23
10801741231305CentroVena One1K0R73161K0R73162026-01-23
10801741231312CentroVena One1K0R73201K0R73202026-01-23
10801741231329CentroVena One1K0R73301K0R73302026-01-23
10801741231336CentroVena One1MB0R72161MB0R72162026-01-23

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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20850026037177PUMA-G Pediatric System™Coaptech, Inc.KGC2025-12-23
10850026037231PUMA-G System™Coaptech, Inc.KGC2024-10-29
10860312001556PUMA-G System™Coaptech, Inc.KGC2024-10-29
10850026037330PUMA-G System™Coaptech, Inc.KGC2024-05-16
00860312001542PUMA-G System™Coaptech, Inc.KGC2024-05-16
00850026037319PUMA-G System™Coaptech, Inc.KGC2024-05-09
00850026037227PUMA-G System™Coaptech, Inc.KGC2024-02-13
00850026037272PUMA-G System™Coaptech, Inc.KGC2024-02-13
00850026037098PUMA-G System™Coaptech, Inc.KGC2023-12-15
00850026037074PUMA-G System™Coaptech, Inc.KGC2023-12-15
00860312001504PUMA-G System™Coaptech, Inc.KGC2023-07-13
00850026037036PUMA-G System™Coaptech, Inc.KGC2023-07-13
00850026037081PUMA-G System™Coaptech, Inc.KGC2023-07-13
10850026037187PUMA-G System™Coaptech, Inc.KGC2023-07-13
10850026037132PUMA-G System™Coaptech, Inc.KGC2023-07-13
00842071131777Decompression TubeAPPLIED MEDICAL TECHNOLOGY, INC.KGC2023-06-30
00842071131463Decompression TubeAPPLIED MEDICAL TECHNOLOGY, INC.KGC2023-06-30
00842071131814Decompression TubeAPPLIED MEDICAL TECHNOLOGY, INC.KGC2023-06-30
00842071131838Decompression TubeAPPLIED MEDICAL TECHNOLOGY, INC.KGC2023-06-30
00842071131852Decompression TubeAPPLIED MEDICAL TECHNOLOGY, INC.KGC2023-06-30
00842071131180ATLAS Suture Delivery SystemAPPLIED MEDICAL TECHNOLOGY, INC.KGC2021-11-15
00842071131203ATLAS Suture Delivery SystemAPPLIED MEDICAL TECHNOLOGY, INC.KGC2021-11-15
07290018632017Low Profile Enteral Feeding Device Kit FIDMI MEDICAL LTDKGC2021-08-15
07290018632024Low Profile Enteral Feeding Device Kit FIDMI MEDICAL LTDKGC2021-08-15
07290018632031Low Profile Enteral Feeding Device Kit FIDMI MEDICAL LTDKGC2021-08-15
07290018632048Low Profile Enteral Feeding Device KitFIDMI MEDICAL LTDKGC2021-08-15
07290018632055Low Profile Enteral Feeding Device Kit FIDMI MEDICAL LTDKGC2021-08-15
00350770102269AVANOSAvanos Medical, Inc.KGC2020-05-23
00350770102290AVANOSAvanos Medical, Inc.KGC2020-05-23