FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M3848133420 · Model: 81-3342 · Bioplate, Inc.
Product Codes
4
GMDN Terms
5
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Bioplate®
Primary DI
M3848133420
Version / Model
81-3342
Catalog Number
81-3342
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
7
Public Version Date
2025-06-09
Public Version Status
Update
Public Device Record Key
ebf4beff-17ca-4ee0-946f-285b0146e1f0

Device Description

Compact Plus Kit ø1.9mm System

Device Characteristics

Single Use
Yes
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
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
LRZ Screwdriver, Surgical
HTD Forceps
FSM Tray, Surgical, Instrument
JEY Plate, Bone

GMDN Terms

Code Name
12143 Instrument tray, reusable
33968 Surgical screwdriver, reusable
42500 Dressing/utility forceps, tweezers-like, reusable
46638 Craniofacial bone screw, non-bioabsorbable
46642 Craniofacial fixation plate, non-bioabsorbable, non-customized

Identifiers

Type ID
Primary M3848133420