FDA UDI In Commercial Distribution 🇺🇸 United States

Modulus

DI: 00887517839589 · Model: ALPMDLUSTLIFAIMP2 · Nuvasive, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Modulus
Primary DI
00887517839589
Version / Model
ALPMDLUSTLIFAIMP2
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-06
Public Version
6
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
77061e8d-cc60-4787-b36f-02b9f5da4baa

Device Description

Alpha Modulus TLIF-A 14mm Wide Imp

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
No
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
No

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00887517839589

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143579 000