FDA UDI In Commercial Distribution 🇺🇸 United States

DynafitSystem

DI: 03701173705576 · Model: I020000 · NEOSTEO
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DynafitSystem
Primary DI
03701173705576
Version / Model
I020000
Catalog Number
I020000
Company Name
NEOSTEO
Labeler DUNS
261106831
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-15
Public Version
1
Public Version Date
2020-12-23
Public Version Status
New
Public Device Record Key
63028e14-29a4-4a0c-8053-e1062689b996

Device Description

Interphalangeal Joint Fusion Device, Size S, 0°, Sterile

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
Yes
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
61687 Interphalangeal joint arthrodesis implant

Identifiers

Type ID
Primary 03701173705576

Device Sizes

Type Value Unit Text
Device Size Text, specify Size S – 0°

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Device must be stored in a place protected from light and humidity