FDA UDI In Commercial Distribution 🇺🇸 United States

TM "Rehabilitimed" K-1PS XXL

DI: 04823097706053 · Model: K-1PS XXL · REABILITIMED TOV
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TM "Rehabilitimed" K-1PS XXL
Primary DI
04823097706053
Version / Model
K-1PS XXL
Catalog Number
K-1PS XXL
Company Name
REABILITIMED TOV
Labeler DUNS
364875768
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-04
Public Version
1
Public Version Date
2025-05-12
Public Version Status
New
Public Device Record Key
5079fa04-a2f5-4724-a364-6684a67ffd8a

Device Description

The orthopedic device is blue in color, has a dense structure, is a knee orthosis made of aeroprene (aeroprene is a soft, breathable, highly elastic neoprene that has additional perforations over the entire surface, which enhances air and moisture exchange.), anatomically correct shape, with an insert made of a special mesh fabric on the back of the leg. Equipped with a relief limiting silicone ring around the opening for the kneecap, reinforced with two spring stiffening ribs on the side surfaces and cross-shaped fasteners with additional straps and locks.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ITM Cage, Knee

GMDN Terms

Code Name
41065 Knee support orthosis

Identifiers

Type ID
Primary 04823097706053

Customer Contacts

Phone
835 5030395

Device Sizes

Type Value Unit Text
Device Size Text, specify Mid-knee circumference in standing position (cm): 46-50