FDA UDI In Commercial Distribution 🇺🇸 United States

Mepitel®

DI: 07310792907108 · Model: 290799 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mepitel®
Primary DI
07310792907108
Version / Model
290799
Company Name
Mölnlycke Health Care AB
Labeler DUNS
631770658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-21
Public Version
2
Public Version Date
2022-11-23
Public Version Status
Update
Public Device Record Key
83004774-e44e-4616-b47b-ee1f2decef06

Device Description

Mepitel 7,5x10cm, US

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
OMP negative pressure wound therapy Powered suction pump

GMDN Terms

Code Name
46855 Wound-nonadherent dressing, permeable, non-antimicrobial

Identifiers

Type ID
Package 07332551585150
Package 07332551585167
Primary 07310792907108

Customer Contacts

Phone
+46737733775

Premarket Submissions

Submission Number Supplement Number
K161797 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 7.5cm x 10cm