FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00889095059007 · Model: 698.131 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00889095059007
Version / Model
698.131
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-28
Public Version
5
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
cf056ae7-013d-424b-8641-a1d251e5ed9f

Device Description

Tissue Forceps, 1X2 Teeth, 10"

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
No
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
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00889095059007

Customer Contacts