FDA UDI In Commercial Distribution 🇺🇸 United States

Pipeline

DI: 00836462015906 · Model: PED-475-35 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pipeline
Primary DI
00836462015906
Version / Model
PED-475-35
Catalog Number
PED-475-35
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-02-12
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
6ec61208-1c5f-4147-aca8-7e48bf84e2e7

Device Description

Flex Embolization Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OUT Intracranial aneurysm flow diverter

GMDN Terms

Code Name
46352 Bare-metal intracranial vascular stent

Identifiers

Type ID
Primary 00836462015906

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P100018 011

Device Sizes

Type Value Unit Text
Device Size Text, specify Usable Length,209,CM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT