FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00889095169843 · Model: 6102.1020 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00889095169843
Version / Model
6102.1020
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-10
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
57ac9049-1228-4902-bf3a-43d657294738

Device Description

Open Door Distractor

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 00889095169843

Customer Contacts