FDA UDI In Commercial Distribution 🇺🇸 United States

RebarTM

DI: 00847536026872 · Model: 105-5082-130 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RebarTM
Primary DI
00847536026872
Version / Model
105-5082-130
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-19
Public Version
3
Public Version Date
2023-07-14
Public Version Status
Update
Public Device Record Key
0307f3d7-f052-480d-b7d9-b043bb405e62

Device Description

MICRO CATH 105-5082-130 V01 REBAR

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRA Catheter, continuous flush

GMDN Terms

Code Name
10691 Vascular microcatheter

Identifiers

Type ID
Primary 00847536026872

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093750 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius