FDA UDI In Commercial Distribution 🇺🇸 United States

TrellOss™-C SA

DI: 00840067206300 · Model: 138N4043 · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TrellOss™-C SA
Primary DI
00840067206300
Version / Model
138N4043
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
1
Public Version Date
2020-07-09
Public Version Status
New
Public Device Record Key
c1281708-24b7-4240-a2a8-1f573e0a7a92

Device Description

Poly Angle Drill, Self Guided

Device Characteristics

Single Use
No
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
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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00840067206300

Customer Contacts

Phone
317-436-7801