FDA UDI In Commercial Distribution 🇺🇸 United States

Porges Coloplast

DI: 05705243322166 · Model: E80103 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Porges Coloplast
Primary DI
05705243322166
Version / Model
E80103
Catalog Number
E80103
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-20
Public Version
1
Public Version Date
2019-04-29
Public Version Status
New
Public Device Record Key
4f165cbd-27a9-4938-b4ad-daf782f48c9b

Device Description

EASIVAC® / System for collecting pieces of tissue after TURP / Connector - WOLF

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
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FFD EVACUATOR, BLADDER, MANUALLY OPERATED

GMDN Terms

Code Name
11301 Closed-wound/centesis drainage receptacle

Identifiers

Type ID
Package 05708932662161
Primary 05705243322166

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store away from light in a cool and dry place