FDA UDI In Commercial Distribution 🇺🇸 United States

Luja Coude

DI: 05701780263245 · Model: 20102 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Luja Coude
Primary DI
05701780263245
Version / Model
20102
Catalog Number
20102
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
2
Public Version Date
2025-09-08
Public Version Status
Update
Public Device Record Key
8b09edd9-8d05-458e-b106-17c8a3c615c5

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
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
EZD Catheter, straight

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Package 05701780263337
Primary 05701780263245
Package 05701780263429

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 12 French
Device Size Text, specify Tip Type Flex Coudé
Catheter Working Length 12.9 Inch
Catheter Working Length 33 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight. Do not use if package is damaged and consult IFU.