FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00195377104366 · Model: 24270110 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00195377104366
Version / Model
24270110
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-24
Public Version
1
Public Version Date
2022-09-01
Public Version Status
New
Public Device Record Key
d307dbec-5531-4c08-b2ec-ab502523c2a3

Device Description

RELINE-ONE Stylet Nav, 110mm Vector

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
64192 Internal spinal fixation procedure kit, reusable

Identifiers

Type ID
Primary 00195377104366

Customer Contacts