Walrus

Primary DI
00857545008011
Brand
Walrus
Company
Q'APEL MEDICAL LLC
Model
FG 00100-01
Catalog number
BG8087-090
Device description
087 Balloon Guide Catheter System, 90cm
Published
2021-06-29
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DQYCatheter, Percutaneous
MJNCatheter, Intravascular Occluding, Temporary

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQYCatheter, PercutaneousCardiovascular2
MJNCatheter, Intravascular Occluding, TemporaryCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K192525000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K192525000087 Balloon Guide Catheter SystemQ'Apel Medical, LLC2019-10-31DQY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00857545008011PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00857545008011008575450080118575450080110857545008011

GMDN Terms#

Term, Definition table
TermDefinition
Vascular guide-catheter, single-useA 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 can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
020937374
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00857545008028WalrusFG 00100-02BG8087-0952021-06-29
008575450080806F ArmadilloFG 00735-052023-08-04
00857545008004WahooFG 00074SF7072-1052021-06-29
00857545008394ZebraAC6074-095AC6074-0952026-03-05
00857545008400ZebraAC6074-105AC6074-1052026-03-05
00857545008431ZebraAC7087-095AC7087-0952026-03-05
00857545008448ZebraAC7087-105AC7087-1052026-03-05
00857545008097072 Aspiration SystemFG 00806AP6072-1322023-10-11
00857545008103072 Aspiration SystemFG 00995APT-952023-10-11
00857545008127072 Aspiration SystemFG 01252APT6072-1322023-10-11
00857545008158ZebraAC6074-095-30AC6074-095-302025-01-03
00857545008165ZebraAC6074-105-30AC6074-105-302025-01-03
00857545008172ZebraAC6074-115-30AC6074-115-302025-01-03
00857545008189ZebraAC6074-095-20AC6074-095-202025-01-03
00857545008196ZebraAC6074-105-20AC6074-105-202025-01-03
00857545008202ZebraAC6074-115-20AC6074-115-202025-01-03
00857545008219ZebraAC7087-095-20-SAC7087-095-20-S2025-01-03
00857545008226ZebraAC7087-105-20-SAC7087-105-20-S2025-01-03
00857545008233ZebraAC7087-095-20-BAC7087-095-20-B2025-01-03
00857545008240ZebraAC7087-105-20-BAC7087-105-20-B2025-01-03

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