FDA UDI In Commercial Distribution 🇺🇸 United States

TrellOss™

DI: 00840067201114 · Model: 231M1008 · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TrellOss™
Primary DI
00840067201114
Version / Model
231M1008
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-09
Public Version
1
Public Version Date
2019-05-17
Public Version Status
New
Public Device Record Key
403a34c4-6bd5-4b5a-9618-a13dff6195ee

Device Description

Paddle Distractor 8mm

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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00840067201114

Customer Contacts

Phone
317-436-7801

Device Sizes

Type Value Unit Text
Width 8 Millimeter