FDA UDI In Commercial Distribution 🇺🇸 United States

Mepiform®

DI: 07323190308309 · Model: 293199 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mepiform®
Primary DI
07323190308309
Version / Model
293199
Company Name
Mölnlycke Health Care AB
Labeler DUNS
631770658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-03
Public Version
2
Public Version Date
2022-11-23
Public Version Status
Update
Public Device Record Key
02f7990e-e3f5-4427-9ee0-d62d2c620558

Device Description

Mepiform 4x30 cm

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
Yes
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
MDA Elastomer, silicone, for scar management

GMDN Terms

Code Name
47772 Scar management dressing, single-use, sterile

Identifiers

Type ID
Package 07332551585686
Package 07332551585693
Primary 07323190308309

Customer Contacts

Phone
+46737733775

Device Sizes

Type Value Unit Text
Device Size Text, specify 4cm x 30cm