FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694098038 · Model: 110-1000-SP-02 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694098038
Version / Model
110-1000-SP-02
Catalog Number
110-1000-SP-02
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b531bf48-861d-485f-b4fc-e10bf34a2149

Device Description

Replacement Battery, Sterile, 2-Pack

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMW HANDPIECE, ROTARY BONE CUTTING

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00845694098038

Customer Contacts

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

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Special Storage Condition, Specify
Special Conditions
Keep dry