FDA UDI In Commercial Distribution 🇺🇸 United States

ASSURE

DI: 00849044000184 · Model: 110.914 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ASSURE
Primary DI
00849044000184
Version / Model
110.914
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-07
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
28af65f6-8692-4833-b97e-f396b5e66632

Device Description

4.5mm Standard Screw, Self-Tapping, 14mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00849044000184

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040721 000

Device Sizes

Type Value Unit Text
Outer Diameter 4.5 Millimeter
Length 14 Millimeter