FDA UDI In Commercial Distribution 🇺🇸 United States

Mölnlycke® Z-Flex™ Fluidized Heel Boot

DI: 07323190250554 · Model: 1400123 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mölnlycke® Z-Flex™ Fluidized Heel Boot
Primary DI
07323190250554
Version / Model
1400123
Company Name
Mölnlycke Health Care AB
Labeler DUNS
631770658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-13
Public Version
1
Public Version Date
2022-12-21
Public Version Status
New
Public Device Record Key
fe5fa0fd-1122-4ca3-b548-4f140497cbe5

Device Description

Fluidized Heel Boot

Device Characteristics

Single Use
No
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
FMP Protector, skin pressure

GMDN Terms

Code Name
36295 Foot friction/impact protector

Identifiers

Type ID
Package 07323190249558
Primary 07323190250554

Customer Contacts

Phone
+46737733775

Device Sizes

Type Value Unit Text
Device Size Text, specify One size