FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694014977 · Model: 220-0049 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694014977
Version / Model
220-0049
Catalog Number
220-0049
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-22
Public Version
3
Public Version Date
2020-01-28
Public Version Status
Update
Public Device Record Key
93351bda-4c65-4f12-a61e-ab8d60c86194

Device Description

Plate Bending Forceps

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
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
46751 Bone holding forceps

Identifiers

Type ID
Primary 00845694014977

Customer Contacts

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

Device Sizes

Type Value Unit Text
Length 6.16 Inch