FDA UDI In Commercial Distribution 🇺🇸 United States

Kolibri

DI: 05701780271998 · Model: RMA110 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kolibri
Primary DI
05701780271998
Version / Model
RMA110
Catalog Number
RMA110
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-20
Public Version
1
Public Version Date
2023-01-30
Public Version Status
New
Public Device Record Key
c02f8b80-ebe5-4edb-868a-5f450b8c6e83

Device Characteristics

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

GMDN Terms

Code Name
60755 Urological surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 05701780272001
Primary 05701780271998
Package 05701780272018

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K211911 000

Device Sizes

Type Value Unit Text
Catheter Gauge 10 French