FDA UDI In Commercial Distribution 🇺🇸 United States

BioBrace

DI: 10653405990154 · Model: BB40X60-FA · Conmed Corporation
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BioBrace
Primary DI
10653405990154
Version / Model
BB40X60-FA
Catalog Number
BB40X60-FA
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-20
Public Version
2
Public Version Date
2026-03-16
Public Version Status
Update
Public Device Record Key
a9319347-7dfa-4079-aa38-33e268d9785b

Device Description

BioBrace® Reinforced Implant, Foot & Ankle, 40 x 60 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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OWY Mesh, surgical, collagen, orthopaedics, reinforcement of tendon
OWW Mesh, surgical, absorbable, orthopaedics, reinforcement of tendon

GMDN Terms

Code Name
60907 Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial

Identifiers

Type ID
Package 20653405990151
Primary 10653405990154

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K241906 000

Device Sizes

Type Value Unit Text
Length 60 Millimeter
Width 40 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius