FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694004480 · Model: 216-1000 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694004480
Version / Model
216-1000
Catalog Number
216-1000
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-04-07
Public Version
3
Public Version Date
2019-09-23
Public Version Status
Update
Public Device Record Key
217244c7-e5c0-46b9-9930-1580f0d3e6fb

Device Description

Logic Jr. Distractor, Left 52mm

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
MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 00845694004480

Customer Contacts

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

Device Sizes

Type Value Unit Text
Device Size Text, specify Distraction Curve Radius = 52mm