FDA UDI In Commercial Distribution 🇺🇸 United States

Purilon

DI: 05701780706124 · Model: 3906 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Purilon
Primary DI
05701780706124
Version / Model
3906
Catalog Number
3906
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-30
Public Version
1
Public Version Date
2022-12-08
Public Version Status
New
Public Device Record Key
799e960a-65be-4735-bb95-56844dab95b5

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAE Dressing, wound, hydrogel without drug and/or biologic

GMDN Terms

Code Name
47764 Wound hydrogel dressing, non-antimicrobial

Identifiers

Type ID
Package 00762123028322
Package 00762123028315
Primary 05701780706124

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Weight - oz 0.28
Weight 8 Gram

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius