FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M3848131050 · Model: 81-3105 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bioplate®
Primary DI
M3848131050
Version / Model
81-3105
Catalog Number
81-3105
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-23
Public Version
7
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
030690b4-b273-4bb0-a6e2-d249520a2eb5

Device Description

1.5mm diam. Plate & Screw Container

Device Characteristics

Single Use
No
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
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
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary M3848131050

Customer Contacts

Phone
888-246-7528

Device Sizes

Type Value Unit Text
Length 7.62 Inch