FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M384K248500 · Model: K248-50 · Bioplate, Inc.
Product Codes
6
GMDN Terms
5
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Bioplate®
Primary DI
M384K248500
Version / Model
K248-50
Catalog Number
K248-50
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-22
Public Version
3
Public Version Date
2024-06-03
Public Version Status
Update
Public Device Record Key
400ec30b-0f42-4824-acc6-e725d2336025

Device Description

Maxfax Set Basic

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
DZA Drill, Dental, Intraoral
HTD Forceps
FZT Cutter, Surgical
LRZ Screwdriver, Surgical
FSM Tray, Surgical, Instrument
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
12143 Instrument tray, reusable
33968 Surgical screwdriver, reusable
42500 Dressing/utility forceps, tweezers-like, reusable
43390 Fluted surgical drill bit, single-use
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary M384K248500