FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M3848133041 · Model: 81-3304 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Bioplate®
Primary DI
M3848133041
Version / Model
81-3304
Catalog Number
81-3304
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
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
a942a523-a874-493b-b94d-d0d1beada69c

Device Description

Screw - Ø1.9 mm x 4.5 mm [50 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 M3848133041
Unit of Use M3848133000

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K980983 000

Device Sizes

Type Value Unit Text
Length 4.5 Millimeter