Unique device identifiers (GUDID)

MICRUSFRAME · MFR141016

Cerenovus, Inc. · MICRUSFRAME C Microcoil 14 Stretch Resistant Coil and Detachable Coil System Contents: 1 Detachable Coil System Coil Ty…

DI 10886704079279RxIn Commercial DistributionHCG
Open FDA's page for this record
Has donation ID number
false
Mri safety
MR Conditional
Record status
Published
Is labeled as nrl
false
Is rx
true
Commercial distribution status
In Commercial Distribution
Public device record key
ed285b5e-1b18-4bb7-b86f-3ca6600e3518
Has serial number
false
Public version date
2026-08-03
Is direct marking exempt
false
Public version number
6
Labeler duns number
607846297
Is labeled as no nrl
false
Is single use
true
Is otc
false
Version or model number
MFR141016
Has manufacturing date
false
Brand name
MICRUSFRAME
Is combination product
false
Is kit
false
Device count in base package
1
Is pm exempt
false
Has lot or batch number
true
Catalog number
MFR141016
Company name
Cerenovus, Inc.
Public version status
Update
Has expiration date
true
Is hct p
false
Publish date
2016-11-16
Device description

MICRUSFRAME C Microcoil 14 Stretch Resistant Coil and Detachable Coil System Contents: 1 Detachable Coil System Coil Type: MICRUSFRAME C 14 Stretch Resistant Coil 10mm (coil diameter) x 16cm (coil length) 190cm (working length)

Sterilization
Is sterile
true
Is sterilization prior use
false
Identifiers
  1. ID
    10886704079279
    Type
    Primary
    Issuing agency
    GS1
Product codes
  1. Code
    HCG
    Name
    DEVICE, NEUROVASCULAR EMBOLIZATION
    Harmonized identifiers (openFDA)
    Device name
    Device, Neurovascular Embolization
    Medical specialty description
    Neurology
    Regulation number
    882.5950
    Device class
    2
  2. Code
    KRD
    Name
    Device, Vascular, for Promoting Embolization
    Harmonized identifiers (openFDA)
    Device name
    Device, Vascular, For Promoting Embolization
    Medical specialty description
    Cardiovascular
    Regulation number
    870.3300
    Device class
    2
Customer contacts
  1. Phone
    +1(800)255-2500
    Email
    xx@xx.xx
Gmdn terms
  1. Code
    60940
    Name
    Neurovascular embolization coil
    Implantable
    true
    Code status
    Active
    Definition

    A 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.

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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.