FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M384SCE413051 · Model: SCE4-13-05 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Bioplate®
Primary DI
M384SCE413051
Version / Model
SCE4-13-05
Catalog Number
SCE4-13-05
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2015-12-03
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e8ce3855-6e81-4973-aaa0-2cb9990f1f3c

Device Description

Emergency Screw - Ø2.3 mm x 13 mm [5 PK]

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
46879 Cranioplasty plate screw

Identifiers

Type ID
Primary M384SCE413051
Unit of Use M384SCE413050

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K953273 000

Device Sizes

Type Value Unit Text
Length 13 Millimeter