FDA UDI In Commercial Distribution 🇺🇸 United States

Liko Original HighBack Sling™, Mod. 200

DI: 00887761982994 · Model: 35200116 · Liko AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Liko Original HighBack Sling™, Mod. 200
Primary DI
00887761982994
Version / Model
35200116
Company Name
Liko AB
Labeler DUNS
354818510
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-10
Public Version
2
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
01eb06e6-685f-4937-bf39-e4edb207b20a

Device Description

Patient lifting system divided leg sling

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
Yes
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
33476 Patient lifting system divided leg sling

Identifiers

Type ID
Primary 00887761982994

Customer Contacts