FDA UDI In Commercial Distribution 🇺🇸 United States

Bioplate®

DI: M3848110430 · Model: 81-1043 · Bioplate, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Bioplate®
Primary DI
M3848110430
Version / Model
81-1043
Catalog Number
81-1043
Company Name
Bioplate, Inc.
Labeler DUNS
838734093
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
7
Public Version Date
2025-06-09
Public Version Status
Update
Public Device Record Key
0a59e9b4-302e-4ed8-ae72-f6a9d4071c2f

Device Description

BioMesh® 3MC - 100 x 150 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
46642 Craniofacial fixation plate, non-bioabsorbable, non-customized

Identifiers

Type ID
Primary M3848110430

Customer Contacts

Phone
888-246-7528

Premarket Submissions

Submission Number Supplement Number
K023665 000

Device Sizes

Type Value Unit Text
Length 150 Millimeter