FDA.reportPublic FDA data

OptiSeal™

Primary DI
20821329001080
Brand
OptiSeal™
Company
Greatbatch Ltd
Model
1003975-009
Catalog number
1003975-009
Device description
Valved Peelable PTFE Introducer
Published
2019-08-15
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20821329001080PackageGS15In Commercial Distribution
00821329001086PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2082132900108020821329001080
00821329001086008213290010868213290010860821329001086

GMDN Terms#

Term, Definition table
TermDefinition
Vascular catheter introduction set, nonimplantableA collection of sterile, nonimplantable, invasive devices intended to provide percutaneous vascular access to enable introduction of a catheter (not included) into the vascular system. It includes a non-steerable introducer sheath with an inner obturator/dilator, and typically an additional access device(s) [e.g., guidewire, introducer needle, syringe, additional dilators] which may include a haemostatic valve to control blood loss, usually to enable arterial access. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Catheter Gauge7French
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
968623467
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
00821329000416Greatbatch Steerable Sheath10876-00110876-0012017-10-19
00821329000423Greatbatch Steerable Sheath10876-00210876-0022017-10-19
00821329000669Boston Scientific Channel Steerable SheathM004CS200M004CS2002018-02-06
00821329401008MOBICATH™D140011D1400112018-02-06
08714729862413Boston Scientific Channel Steerable SheathM004CS100M004CS1002016-09-24
08714729862420Boston Scientific Channel Steerable SheathM004CS200M004CS2002016-09-24
00846835012371MobiCath™D140011D1400112016-09-24
00846835012388MobiCath™D140010D1400102016-09-24
00821329000652Boston Scientific Channel Steerable SheathM004CS100M004CS1002018-02-06
00821329400995MOBICATH™D140010D1400102018-02-06
00821329601491Greatbatch Steerable Sheath10876-00110876-0012016-09-24
00821329601507Greatbatch Steerable Sheath10876-00210876-0022016-09-24
00821329580499Algovita®5208-20-USA5208-202015-12-01
00821329580505Algovita®5208-40-USA5208-402015-12-01
00821329580512Algovita®5208-60-USA5208-602015-12-01
00821329580529Algovita®5212-20-USA5212-202015-12-01
00821329580536Algovita® 5212-40-USA5212-402015-12-01
00821329580543Algovita® 5212-60-USA5212-602015-12-01
00821329900204Myopore® Sutureless Myocardial Pacing Lead5112102015-05-21
00821329900228Myopore® Sutureless Myocardial Pacing Lead5112122015-05-21

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Primary DI, Brand, Company table
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