FDA UDI In Commercial Distribution 🇺🇸 United States

NewPort™

DI: 10889981013141 · Model: NWPIMP · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NewPort™
Primary DI
10889981013141
Version / Model
NWPIMP
Catalog Number
NWPIMP
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4b06d8c8-f365-42bb-ad4b-1115d0a2355a

Device Description

NewPort Implant Tray

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10889981013141

Customer Contacts