FDA UDI In Commercial Distribution 🇺🇸 United States

Biogel® Skinsense® Indicator® System

DI: 05060097937615 · Model: 40685 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Biogel® Skinsense® Indicator® System
Primary DI
05060097937615
Version / Model
40685
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
4
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
d3e010c7-6e10-42d0-ac23-9aa4d47ccbb3

Device Description

Biogel Skinsense Underglove 8.5x50

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
KGO Surgeon's gloves

GMDN Terms

Code Name
57970 Polychloroprene surgical glove, non-powdered

Identifiers

Type ID
Package 05060097937776
Package 05060097937691
Primary 05060097937615

Customer Contacts

Phone
+46737733775

Device Sizes

Type Value Unit Text
Device Size Text, specify 8.5