FDA UDI In Commercial Distribution 🇺🇸 United States

Solo Octo LiftSheet™

DI: 00887761984202 · Model: 3683905 · Liko AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Solo Octo LiftSheet™
Primary DI
00887761984202
Version / Model
3683905
Company Name
Liko AB
Labeler DUNS
354818510
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-22
Public Version
2
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
cf8eb606-655f-4099-8fdd-d45aa6c0a340

Device Description

Patient lifting system stretcher

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FSA Lift, patient, non-ac-powered

GMDN Terms

Code Name
40536 Patient lifting system stretcher

Identifiers

Type ID
Package 10887761984209
Primary 00887761984202

Customer Contacts