FDA UDI In Commercial Distribution 🇺🇸 United States

PMMA

DI: 00887517303271 · Model: 6280132 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PMMA
Primary DI
00887517303271
Version / Model
6280132
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-04
Public Version
1
Public Version Date
2019-12-12
Public Version Status
New
Public Device Record Key
a7e97ec5-94cd-4b67-a6a4-83038a3333a6

Device Description

PMMA Needle, Packaged Design 2

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00887517303271

Customer Contacts