FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694043700 · Model: 213-1620 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694043700
Version / Model
213-1620
Catalog Number
213-1620
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
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
ac3c0a7d-5d19-48ed-8676-853e3664ff5c

Device Description

LPM Mesh, 93mm x 93mm x 0.6mm, Rigid

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
JEY PLATE, BONE

GMDN Terms

Code Name
46642 Craniofacial fixation plate, non-bioabsorbable, non-customized

Identifiers

Type ID
Primary 00845694043700

Customer Contacts

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

Device Sizes

Type Value Unit Text
Length 93 Millimeter