FDA UDI In Commercial Distribution 🇺🇸 United States

Vitality®

DI: 00887868153952 · Model: 705M1190 · BIOMET SPINE LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitality®
Primary DI
00887868153952
Version / Model
705M1190
Catalog Number
705M1190
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-15
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
c7f4c32a-08f6-4595-9754-28a5d8b7a6a8

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, fixation, spinal intervertebral body
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00887868153952

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify POLYAXIAL CLOSED ILIAC SCREW, Ø11.0MM X 90MM