HeartSpan®

Primary DI
10884450169114
Brand
HeartSpan®
Company
Merit Medical
Model
00884450169117
Catalog number
FCL-160-01
Published
2018-06-11
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DYBINTRODUCER, CATHETER

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DYBIntroducer, CatheterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K132720000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K132720000HEARTSPAN FIXED CURVE BRAIDED TRANSSEPTAL SHEATHMerit Medical Systems, Inc.2014-02-12DYB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10884450169114PackageGS15In Commercial Distribution
00884450169117PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088445016911410884450169114
00884450169117008844501691178844501691170884450169117

GMDN Terms#

Term, Definition table
TermDefinition
Cardiac transseptal access setA collection of nonimplantable, invasive devices intended to be used to puncture the interatrial septum during a transseptal catheterization procedure, and to create a conduit for the introduction of various cardiovascular catheters into the left side of the heart. It includes a vascular guide-catheter (which may be referred to as a steerable introducer) with a transseptal needle to create the puncture, and typically includes additional introduction assistive devices necessary for the procedure (e.g., stylet, guidewire, dilator). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
065673912
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
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10884450313654Prelude Prestige™10884450313654PLPS-25162020-07-16
10884450313739Prelude Prestige™10884450313739PLPS-10082021-04-09
10884450313760Prelude Prestige™10884450313760PLPS-25102020-06-02
10884450313791Prelude Prestige™10884450313791PLPS-25082020-06-02
10884450313807Prelude Prestige™10884450313807PLPS-10102021-04-09
10884450313821Prelude Prestige™10884450313821PLPS-25072020-07-16
10884450313838Prelude Prestige™10884450313838PLPS-10112021-04-09
10884450313852Prelude Prestige™10884450313852PLPS-10122021-04-09
10884450313869Prelude Prestige™10884450313869PLPS-25052020-07-16
10884450495565Hydrophilic Prelude SNAP™10884450495565PLSH-1009.5/A2021-11-22
00884450161944SafeSheath CSG00884450161944CSG-90-092017-03-14
00884450161951SafeSheath CSG00884450161951FCL-069-002017-02-20
00884450161975SafeSheath CSG00884450161975FCL-069-022018-01-15
00884450161982SafeSheath CSG00884450161982FCL-069-032017-05-24
00884450161999SafeSheath CSG00884450161999FCL-070-002017-05-08
00884450162002SafeSheath CSG00884450162002FCL-070-012017-10-16
00884450162033SafeSheath CSG00884450162033FCL-083-002017-02-15
00884450162040SafeSheath CSG00884450162040FCL-083-012017-02-15
00884450162057SafeSheath CSG00884450162057FCL-083-022017-02-15
00884450162064SafeSheath CSG00884450162064FCL-083-032017-02-15

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Primary DI, Brand, Company table
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08498840011812VYGONVygon CorporationDYB2019-04-08
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