FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M384SCD204501 · Model: SCD2-04-50 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

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Basic Information

Brand Name
Bioplate®
Primary DI
M384SCD204501
Version / Model
SCD2-04-50
Catalog Number
SCD2-04-50
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-10-30
Public Version
5
Public Version Date
2024-06-19
Public Version Status
Update
Public Device Record Key
a2a2c726-b883-40a8-8655-4d9e181ebbf9

Device Description

Self-Drilling Screw - Ø1.5 mm x 4 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
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M384SCD204501
Unit of Use M384SCD204500

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K022890 000

Device Sizes

Type Value Unit Text
Length 4 Millimeter