FDA UDI In Commercial Distribution 🇺🇸 United States

Trulife

DI: 00755517852719 · Model: 0800502 · TRULIFE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trulife
Primary DI
00755517852719
Version / Model
0800502
Company Name
TRULIFE LIMITED
Labeler DUNS
289728891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-31
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
01248d5f-2b16-4d19-902b-1589594c6ac6

Device Description

STRAP GRIP KIT SM/MD SPINAL HYPEREXTENSION T34/T37/T39/T39S

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MRI ORTHOSIS, TRUNCAL/ORTHOSIS, LIMB

GMDN Terms

Code Name
41042 Thoracic spine orthosis

Identifiers

Type ID
Primary 00755517852719