FDA UDI In Commercial Distribution 🇺🇸 United States

BioPatch®

DI: 20705031132907 · Model: 44151 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
BioPatch®
Primary DI
20705031132907
Version / Model
44151
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-06-20
Public Version
8
Public Version Date
2023-05-16
Public Version Status
Update
Public Device Record Key
253a8207-c17f-4363-aaba-c76f6cf501d0

Device Description

BioPatch® Protective Disk with CHG

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRO Dressing, wound, drug

GMDN Terms

Code Name
48124 Exudate-absorbent dressing, non-gel, antimicrobial

Identifiers

Type ID
Package 30705031132904
Primary 20705031132907
Unit of Use 10705031132900

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003229 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.9 cm (0.75in) circumference; 1.5mm center hole

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius