FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00842528104064 · Model: 316-1904 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00842528104064
Version / Model
316-1904
Catalog Number
316-1904
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-17
Public Version
8
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
d25271cb-5b1c-4272-89c3-ef0a9066518f

Device Description

ExtremiFix Large, 7.0mm Headless Screw Module

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
Yes
Has Lot/Batch Number
No
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00842528104064

Customer Contacts

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

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Stored at controlled room temperature