FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694065504 · Model: 218-0092-SP-10 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694065504
Version / Model
218-0092-SP-10
Catalog Number
218-0092-SP-10
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-02
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
b5e07a26-9af0-46d0-82a8-6d3efd4b13d6

Device Description

1.6 System Low Profile Medium Straight Plate Sterile Qty 10

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
46642 Craniofacial fixation plate, non-bioabsorbable, non-customized

Identifiers

Type ID
Primary 00845694065504

Customer Contacts

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

Device Sizes

Type Value Unit Text
Length 14 Millimeter