FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M384813050CP1 · Model: 81-3050-CP · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Bioplate®
Primary DI
M384813050CP1
Version / Model
81-3050-CP
Catalog Number
81-3050-CP
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-02-25
Public Version
4
Public Version Date
2024-02-26
Public Version Status
Update
Public Device Record Key
8e117b9e-d6a2-4a0b-aef7-4d7b2fc80bb7

Device Description

Screw - Ø1.9 mm x 4 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
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
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M384813050CP1
Unit of Use M384813050CP0

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K980983 000

Device Sizes

Type Value Unit Text
Length 4 Millimeter