FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694094658 · Model: 231-2828T · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694094658
Version / Model
231-2828T
Catalog Number
231-2828T
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b9b4f64a-10e3-4212-9cc8-8e5e96cd02b8

Device Description

Large, Prebent Recon TEMPLATE, ICON

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00845694094658

Customer Contacts

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

Device Sizes

Type Value Unit Text
Length 188 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at controlled room temperature out of direct sunlight