FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00887517627032 · Model: 10000896 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00887517627032
Version / Model
10000896
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
349ba28f-a06c-4829-903d-5ce3c2058410

Device Description

RELINE HS Pedicle Elevator, 8mm

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
35048 Bone lever/elevator, reusable

Identifiers

Type ID
Primary 00887517627032

Customer Contacts