FDA UDI In Commercial Distribution 🇺🇸 United States

TLIF/PLIF Disc Prep

DI: 00190837086848 · Model: 112-493 · Life Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TLIF/PLIF Disc Prep
Primary DI
00190837086848
Version / Model
112-493
Catalog Number
112-493
Company Name
Life Spine, Inc.
Labeler DUNS
183641617
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-07
Public Version
1
Public Version Date
2019-11-15
Public Version Status
New
Public Device Record Key
7f4457b4-142d-49ce-8b6a-7abb6cd35fb8

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
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary 00190837086848