FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00887517730701 · Model: 10001029 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00887517730701
Version / Model
10001029
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-02
Public Version
4
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
ecae1e44-1582-4d45-b153-eb9e5d0e6070

Device Description

RELINE ConSol Disp Kit, Bevel Tip- 1pk

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ETN STIMULATOR, NERVE

GMDN Terms

Code Name
35886 Body aspiration needle, single-use

Identifiers

Type ID
Primary 00887517730701

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K112709 000