FDA UDI Not in Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694040396 · Model: 812-0113 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694040396
Version / Model
812-0113
Catalog Number
812-0113
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9d15fd3e-e115-45cf-b803-04e3ce1dee43
Distribution End Date
2017-12-29

Device Description

PrimaLIF LLIF 13mm Box Osteotome

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
Yes
PM Exempt
No
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00845694040396

Customer Contacts

Phone
+1(800)456-7779 ext. 1