FDA UDI In Commercial Distribution 🇺🇸 United States

AlligatorTM

DI: 00847536014039 · Model: FA-88810-50 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AlligatorTM
Primary DI
00847536014039
Version / Model
FA-88810-50
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-05
Public Version
3
Public Version Date
2021-07-08
Public Version Status
Update
Public Device Record Key
f0a838e1-a1a2-4894-a52f-be8a6990aca9

Device Description

FA-88810-50 ALLIGATOR DEVICE ARD 5MM

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
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17927 Intravascular extraction catheter-snare

Identifiers

Type ID
Primary 00847536014039

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid temperature extremes, keep dry, keep away from sunlight