FDA.reportPublic FDA data

CELLO™, Balloon Guide Catheter

Primary DI
04544050093491
Brand
CELLO™, Balloon Guide Catheter
Company
FUJI SYSTEMS CORPORATION
Model
9F
Catalog number
1610590
Device description
The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures.
Published
2015-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQYCatheter, Percutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K120781000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K120781000CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTHFuji Systems Corp.2012-08-09DQY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04544050093491PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04544050093491045440500934914544050093491

GMDN Terms#

Term, Definition table
TermDefinition
Vascular guide-catheter, single-useA sterile, flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section of the tube can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended for infusion, is not a microcatheter (i.e., not intended to access superselective small vessels), and does not include a transseptal needle. It may include a disposable percutaneous introduction set. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
949-837-3700XX@XX.XX

Regulatory Flags#

DUNS number
715919973
Device count
1
Lot or batch
true
Serial number
true
Expiration date on label
true
Donation ID number
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04544050121057CELLO II Balloon Guide Catheter, 8F 90cm16509082026-05-25
04544050123815UNIVENT TUBE (TCB TYPE)I.D. 8.0MM12029332024-01-31
04544050123839UNIVENT TUBE (TCB TYPE)I.D. 6.0MM12029272024-01-31
04544050123846UNIVENT TUBE (TCB TYPE)I.D. 6.5MM12029282024-01-31
04544050123853UNIVENT TUBE (TCB TYPE)I.D. 7.0MM12029302024-01-31
04544050123860UNIVENT TUBE (TCB TYPE)I.D. 7.5MM12029312024-01-31
04544050123877UNIVENT TUBE (TCB TYPE)I.D. 8.5MM12029352024-01-31
04544050123884UNIVENT TUBE (TCB TYPE)I.D. 9.0MM12029362024-01-31
04544050123891UNIVENT TUBE (TCB TYPE)I.D. 9.5MM12029372024-01-31
04544050123907UNIVENT TUBE (TCB TYPE)I.D. 10.0MM12029392024-01-31
14544050123812UNIVENT TUBE (TCB TYPE)I.D. 8.0MM12029332024-01-31
14544050123836UNIVENT TUBE (TCB TYPE)I.D. 6.0MM12029272024-01-31
14544050123843UNIVENT TUBE (TCB TYPE)I.D. 6.5MM12029282024-01-31
14544050123850UNIVENT TUBE (TCB TYPE)I.D. 7.0MM12029302024-01-31
14544050123867UNIVENT TUBE (TCB TYPE)I.D. 7.5MM12029312024-01-31
14544050123874UNIVENT TUBE (TCB TYPE)I.D. 8.5MM12029352024-01-31
14544050123881UNIVENT TUBE (TCB TYPE)I.D. 9.0MM12029362024-01-31
14544050123898UNIVENT TUBE (TCB TYPE)I.D. 9.5MM12029372024-01-31
14544050123904UNIVENT TUBE (TCB TYPE)I.D. 10.0MM12029392024-01-31
04544050120739CELLO™, Balloon Guide Catheter16105802022-01-18

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