FDA.reportPublic FDA data

HydroFrame 10 Advanced

Primary DI
04987350983596
Brand
HydroFrame 10 Advanced
Company
MICROVENTION INC.
Model
100833HFRM-V-A2
Catalog number
100833HFRM-V
Device description
V-Trak
Published
2018-08-07
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
OTC
false
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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04987350983596PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04987350983596049873509835964987350983596

GMDN Terms#

Term, Definition table
TermDefinition
Neurovascular embolization coilA sterile, non-bioabsorbable, implantable device intended to induce a neurovascular thrombosis to treat an intracranial aneurysm and/or neurovascular arteriovenous malformation (AVM); it may also be intended to treat non-neurovascular malformations. It is in the form of a metal [e.g., platinum alloy] or metal/synthetic polymer wire which coils upon deployment within the aneurysm/vasculature; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.

Device Sizes#

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

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(714)247-8000customerservice@microvention.c

Regulatory Flags#

DUNS number
003263105
Device count
1
DM exempt
true
Premarket exempt
false
HCT/P
false
Kit
false
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
true
Sterilization required before use
false

Other Devices From This Company#

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30816777025907Tubing Kit - StrokeMVTK110MVTK1102021-11-26
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10810170018098Azur Pure Helical45-08030245-0803022015-12-29
10810170018104Azur Pure Helical45-08030445-0803042015-12-29
10810170018111Azur Pure Helical45-08030645-0803062015-12-29
10810170018128Azur Pure Helical45-08040245-0804022015-12-29
10810170018135Azur Pure Helical45-08040445-0804042015-12-29
10810170018142Azur Pure Helical45-08040645-0804062015-12-29
10810170018159Azur Pure Helical45-08041045-0804102015-12-29
10810170018166Azur Pure Helical45-08050445-0805042015-12-29
10810170018173Azur Pure Helical45-08050645-0805062015-12-29
10810170018180Azur Pure Helical45-08051045-0805102015-12-29
10810170018197Azur Pure Helical45-08051445-0805142015-12-29
10810170018203Azur Pure Helical45-08060645-0806062015-12-29
10810170018210Azur Pure Helical45-08061045-0806102015-12-29
10810170018227Azur Pure Helical45-08061445-0806142015-12-29
10810170018234Azur Pure Helical45-08062045-0806202015-12-29
10810170018241Azur Pure Helical45-08081045-0808102015-12-29
10810170018258Azur Pure Helical45-08081445-0808142015-12-29

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10857798005123Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
10857798005130Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
10857798005147Nitinol Enhanced DeviceEmbolization Inc.KRD2026-02-12
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10841156100001OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27
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10841156100025OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27
10841156100032OPTISPHERETELEFLEX INCORPORATEDKRD2018-03-27