FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M384P2SB0214501 · Model: P2SB-02-14-50 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Bioplate®
Primary DI
M384P2SB0214501
Version / Model
P2SB-02-14-50
Catalog Number
P2SB-02-14-50
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-10-29
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
64e20ebe-5a62-4049-b051-fde1182132af

Device Description

Straight Plate - Ø1.5 mm - 2 hole - 14 mm (50PK)

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
No
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 M384P2SB0214501
Unit of Use M384P2SB0214500

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K002426 000

Device Sizes

Type Value Unit Text
Length 14 Millimeter