FDA UDI In Commercial Distribution 🇺🇸 United States

Trulife

DI: 00645517852720 · Model: T37T39PADKIT · TRULIFE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trulife
Primary DI
00645517852720
Version / Model
T37T39PADKIT
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
2
Public Version Date
2023-06-08
Public Version Status
Update
Public Device Record Key
fc2fa871-5a06-4410-a13b-f9db8c0ec37a

Device Description

PAD KIT SPINAL HYPERXTENSION 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 00645517852720