FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780032397 · Model: MWM8101 · Integra Lifesciences Corporation
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780032397
Version / Model
MWM8101
Catalog Number
MWM8101
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
9
Public Version Date
2023-05-16
Public Version Status
Update
Public Device Record Key
15850de3-4e62-44a8-8278-0cb67bea5763

Device Description

Integra® MESHED BILAYER WOUND MATRIX 8 in*10 in (20 cm*25 cm)

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRO Dressing, wound, drug
KGN Dressing, wound, collagen

GMDN Terms

Code Name
45023 Collagen wound matrix dressing

Identifiers

Type ID
Secondary M269MWM81011
Primary 10381780032397

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081635 000

Device Sizes

Type Value Unit Text
Length 25 Centimeter
Length 10 Inch
Width 8 Inch
Width 20 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store Flat
Type
Handling Environment Temperature
Temperature Range
10 – 30 Degrees Celsius