FDA UDI In Commercial Distribution 🇺🇸 United States

X-celeratorTM

DI: 00847536004580 · Model: 103-0602-300 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
X-celeratorTM
Primary DI
00847536004580
Version / Model
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
2016-07-16
Public Version
3
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
1b37ff8a-a132-4f97-ad01-4561f818bf12

Device Description

103-0602-300 XCELERATOR14 GWIRE

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DQX WIRE, GUIDE, CATHETER

GMDN Terms

Code Name
58115 Peripheral vascular guidewire, manual

Identifiers

Type ID
Primary 00847536004580

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit