FDA UDI In Commercial Distribution 🇺🇸 United States

REVERE

DI: 00889095192940 · Model: 231.118 · GLOBUS MEDICAL, INC.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REVERE
Primary DI
00889095192940
Version / Model
231.118
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
2018-07-06
Public Version Status
Update
Public Device Record Key
f4dfd5bd-4f97-45b3-83e3-6fd18c400b5d

Device Description

Stainless Steel Cross Connector, 18mm

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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNH Orthosis, spondylolisthesis spinal fixation
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
37272 Trans-facet-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00889095192940

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061202 000

Device Sizes

Type Value Unit Text
Length 18 Millimeter