FDA.reportPublic FDA data

Prestige Coil System

Primary DI
00840303709275
Brand
Prestige Coil System
Company
BALT USA LLC
Model
PRES0930CPKPL
Catalog number
N/A
Device description
The Prestige Coil System is indicated for arterial and venous embolizations in the peripheral vasculature. It is designed for use with the Ultra Detachment Controller.
Published
2024-11-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KRDDevice, Vascular, For Promoting Embolization

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KRDDevice, Vascular, For Promoting EmbolizationCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K220699000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K220699000Prestige Coil SystemBait USA, LLC2022-04-08KRD

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840303709275PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840303709275008403037092758403037092750840303709275

GMDN Terms#

Term, Definition table
TermDefinition
Non-neurovascular embolization coilA non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store at a controlled room temperature in a dry place.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-949-788-1443customerservice@balt-usa.com

Regulatory Flags#

DUNS number
945543689
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840303712053Prestige Coil SystemPRESPACK30N/A2026-07-14
00840303712077Prestige Coil SystemPRESPACK65N/A2026-07-14
00840303712091Prestige Coil SystemPRESPACK55N/A2026-07-14
00840303712107Prestige Coil SystemPRESPACK55N/A2026-07-14
00840303714521Optima Coil System (OptiOne Coil System)OPTIONE4SN/A2026-07-06
00840303714538Optima Coil System (OptiOne Coil System)OPTIONE4MN/A2026-07-06
00840303714545Optima Coil System (OptiOne Coil System)OPTIONE4LN/A2026-07-06
00840303714552Optima Coil System (OptiOne Coil System)OPTIONE45SN/A2026-07-06
00840303714569Optima Coil System (OptiOne Coil System)OPTIONE45MN/A2026-07-06
00840303714576Optima Coil System (OptiOne Coil System)OPTIONE45LN/A2026-07-06
00840303714583Optima Coil System (OptiOne Coil System)OPTIONE5SN/A2026-07-06
00840303714590Optima Coil System (OptiOne Coil System)OPTIONE5MN/A2026-07-06
00840303714606Optima Coil System (OptiOne Coil System)OPTIONE5LN/A2026-07-06
00840303714613Optima Coil System (OptiOne Coil System)OPTIONE5XLN/A2026-07-06
00840303714620Optima Coil System (OptiOne Coil System)OPTIONE55SN/A2026-07-06
00840303714637Optima Coil System (OptiOne Coil System)OPTIONE55MN/A2026-07-06
00840303714644Optima Coil System (OptiOne Coil System)OPTIONE55LN/A2026-07-06
00840303714651Optima Coil System (OptiOne Coil System)OPTIONE55XLN/A2026-07-06
00840303714668Optima Coil System (OptiOne Coil System)OPTIONE6SN/A2026-07-06
00840303714675Optima Coil System (OptiOne Coil System)OPTIONE6MN/A2026-07-06

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