FDA UDI In Commercial Distribution 🇺🇸 United States

X-celerator

DI: 00836462003071 · Model: 103-0602-300 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
X-celerator
Primary DI
00836462003071
Version / Model
103-0602-300
Catalog Number
103-0602-300
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-06
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0cc0a4df-6eb2-4659-bedc-855b00c4ff0c

Device Description

14 Exchange Hydrophilic Guidewire

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQX WIRE, GUIDE, CATHETER

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Primary 00836462003071

Customer Contacts

Device Sizes

Type Value Unit Text
Length 300 Centimeter
Device Size Text, specify Guidewire,.014,Inch;

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Avoid extreme temperatures;Keep dry;AVOID DIRECT SUNLIGHT