FDA UDI In Commercial Distribution 🇺🇸 United States

Coloplast

DI: 05708932688352 · Model: SUE365 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Coloplast
Primary DI
05708932688352
Version / Model
SUE365
Catalog Number
SUE365
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-03
Public Version
2
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
a1a8d556-08b6-42ee-b92e-3abd059f0ded

Device Description

SabreLine Single Use Laser Fiber 365um

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
GEX Powered laser surgical instrument

GMDN Terms

Code Name
47785 Urogenital surgical laser system beam guide, single-use

Identifiers

Type ID
Package 05708932688369
Primary 05708932688352

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182831 000

Device Sizes

Type Value Unit Text
Outer Diameter 365 Micrometer

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight