FDA UDI In Commercial Distribution 🇺🇸 United States

Biogel® Neoderm®

DI: 07332551891510 · Model: 42960 · Mölnlycke Health Care AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Biogel® Neoderm®
Primary DI
07332551891510
Version / Model
42960
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
abfd8a1a-0274-4b85-8376-873a2ed2e5a1

Device Description

Biogel NeoDerm 6.0x50

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 07332551891497
Package 07332551891503
Primary 07332551891510

Customer Contacts

Phone
+46737733775

Device Sizes

Type Value Unit Text
Device Size Text, specify 6.0