FDA UDI In Commercial Distribution 🇺🇸 United States

Mefix®

DI: 07323190203314 · Model: 310500 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mefix®
Primary DI
07323190203314
Version / Model
310500
Company Name
Mölnlycke Health Care AB
Labeler DUNS
631770658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-02
Public Version
2
Public Version Date
2022-11-23
Public Version Status
Update
Public Device Record Key
92a5785d-0d74-4288-930f-262759578490

Device Description

Mefix 5cm x 10m

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
No
Sterilization Prior Use
No

Product Codes

Code Name
KGX Tape and bandage, adhesive

GMDN Terms

Code Name
16866 Dressing-fixation skin adhesive tape, non-silicone

Identifiers

Type ID
Package 07323190195190
Package 07323190195206
Primary 07323190203314

Customer Contacts

Phone
+46737733775

Device Sizes

Type Value Unit Text
Device Size Text, specify 5cm x 10m