FDA UDI In Commercial Distribution 🇺🇸 United States

VYGON

DI: 03660812152808 · Model: 38.08.06 · VYGON
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VYGON
Primary DI
03660812152808
Version / Model
38.08.06
Catalog Number
00380806
Company Name
VYGON
Labeler DUNS
392994778
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-24
Public Version
1
Public Version Date
2023-08-01
Public Version Status
New
Public Device Record Key
091cea2d-367d-4ce4-a3f8-eb1e699f6ac5

Device Description

Dermafilm 8,5x6cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
KKX Drape, surgical

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 53660812152803
Package 33660812152809
Primary 03660812152808

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius