FDA UDI In Commercial Distribution 🇺🇸 United States

Dymaxeon®

DI: 00815500021697 · Model: 05.5 · BACK 2 BASIC DIRECT, LLC
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Dymaxeon®
Primary DI
00815500021697
Version / Model
05.5
Catalog Number
06.6394B
Company Name
BACK 2 BASIC DIRECT, LLC
Labeler DUNS
043841348
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2016-01-19
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
bb5b5e1b-3f72-48cc-b81c-07ebb4f5eabe

Device Description

DYMAXEON 5.5 OPEN POLYAXIAL PEDICULAR SCREW Ø7,5 x40mm (VIOLET)

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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
MNH Orthosis, spondylolisthesis spinal fixation
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00815500021697
Unit of Use 10815500021694

Customer Contacts

Device Sizes

Type Value Unit Text
Length 40 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
devices kept at room temperature or other standard conditions
Type
Storage Environment Temperature
Temperature Range
High: 86 Degrees Fahrenheit