IOPS™

Primary DI
00843152101030
Brand
IOPS™
Company
Centerline Biomedical, Inc.
Model
RCC-1
Catalog number
RCC-1
Device description
IOPS™ Catheter Reverse Curve 1
Published
2020-09-18
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DQKComputer, Diagnostic, Programmable

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQKComputer, Diagnostic, ProgrammableCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K190106000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K190106000Intra-Operative Positioning System; Simple Curve Catheter, Reverse Curve Catheter ; Angled Tip Guidewire ; Tracking Pad ; Guidewire HandleCenterline Biomedical, Inc.2019-06-24DQK

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10843152101037PackageGS15Not in Commercial Distribution
00843152101030PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1084315210103710843152101037
00843152101030008431521010308431521010300843152101030

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), needle 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.

Regulatory Flags#

DUNS number
080088507
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00843152100002IOPS Mobile CartMC-1MC-12020-09-18
00843152101078IOPS ViewpointC01251C012512024-10-01
00843152101108IOPS ViewpointC00752C007522024-10-01
00843152101115IOPS ViewpointC01252C012522024-10-01
00843152102037IOPS™ATW-2ATW-22020-09-18
00843152102051IOPS®H01035H010352024-11-11
00843152101061IOPS ViewpointC00751C007512024-10-01
00843152100057IOPS Visionary SystemMC-32026-02-24
00843152101023IOPS™SCC-1SCC-12020-09-18
00843152102013IOPS™SSH-1SSH-12020-10-21
00843152103003IOPS™TP-1TP-12020-09-18
00843152103027IOPS®T02111T021112025-03-18
00843152104000IOPS™ Software ApplicationSW-1SW-12020-09-18
10843152102034IOPS™ATW-2ATW-22020-09-18
10843152103024IOPS®T02111T021112025-03-18
10843152102058IOPS®H01035H010352024-11-11
10843152101075IOPS ViewpointC01251C012512024-10-01
10843152101105IOPS ViewpointC00752C007522024-10-01
10843152101112IOPS ViewpointC01252C012522024-10-01
10843152103000IOPS™TP-1TP-12020-09-18

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Primary DI, Brand, Company table
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