FDA UDI In Commercial Distribution 🇺🇸 United States

HyperForm

DI: 00763000294298 · Model: 104-4715 · Micro Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HyperForm
Primary DI
00763000294298
Version / Model
104-4715
Company Name
Micro Therapeutics, Inc.
Labeler DUNS
826110710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-01
Public Version
4
Public Version Date
2025-12-11
Public Version Status
Update
Public Device Record Key
66031a5a-5eb9-440e-8421-17ba2a2ac0a6

Device Description

BALLOON SYSTEM 104-4715 V20 HYPERFORM

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
MJN Catheter, intravascular occluding, temporary

GMDN Terms

Code Name
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00763000294298

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091458 000
K101570 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
This device should be stored in a dry place at between 50°F (10°C) and 90°F (32°C).