FDA UDI Not in Commercial Distribution 🇺🇸 United States

NEOPLATE

DI: 07898624867795 · Model: 942.621 · Neoortho Produtos Ortopédicos S/A.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEOPLATE
Primary DI
07898624867795
Version / Model
942.621
Company Name
Neoortho Produtos Ortopédicos S/A.
Labeler DUNS
914644351
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-25
Public Version
4
Public Version Date
2023-12-19
Public Version Status
Update
Public Device Record Key
6c9138b0-f6fe-4c89-a255-be1f1f3afb96
Distribution End Date
2016-08-25

Device Description

G2 Anterior Cervical Plate 78 mm

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

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 07898624867795

Customer Contacts