FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00842528123300 · Model: 218-3190-SP · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00842528123300
Version / Model
218-3190-SP
Catalog Number
218-3190-SP
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-08
Public Version
1
Public Version Date
2019-11-18
Public Version Status
New
Public Device Record Key
505d3c41-1618-4371-a332-2753452e67c7

Device Description

SmartFlex Spring NC- 9.0N

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PBJ Cranial Distraction System

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 00842528123300

Customer Contacts

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