FDA UDI In Commercial Distribution 🇺🇸 United States

Lumbar Interbody Fusion System (OLLIF) Inserter- Outer

DI: 00850014575045 · Model: 01-00-1 · ADVANCED RESEARCH MEDICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lumbar Interbody Fusion System (OLLIF) Inserter- Outer
Primary DI
00850014575045
Version / Model
01-00-1
Catalog Number
01-00-2
Company Name
ADVANCED RESEARCH MEDICAL LLC
Labeler DUNS
117201206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-23
Public Version
1
Public Version Date
2019-12-31
Public Version Status
New
Public Device Record Key
4dfbe701-0bcf-444d-97f6-ad1f258244d5

Device Description

OLLIF Inserter-Inner

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
Yes
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
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00850014575045

Customer Contacts