FDA UDI In Commercial Distribution 🇺🇸 United States

NewPort

DI: 10889981083809 · Model: 91-8288 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NewPort
Primary DI
10889981083809
Version / Model
91-8288
Catalog Number
91-8288
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4efd2edd-4141-4fd4-a8f2-b39c86ae2ae1

Device Description

520mm SS Guidewire, Double Blunt

Device Characteristics

Single Use
Yes
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
HXS TWISTER, WIRE

GMDN Terms

Code Name
47870 Orthopaedic fixation implant alignment tool

Identifiers

Type ID
Primary 10889981083809

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 520mm