FDA UDI In Commercial Distribution 🇺🇸 United States

A Supreme

DI: 00643293000267 · Model: 503 13R · TRULIFE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
A Supreme
Primary DI
00643293000267
Version / Model
503 13R
Company Name
TRULIFE LIMITED
Labeler DUNS
985048669
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
9008e32f-db62-4f02-a4a1-2328bca00070

Device Description

A Supreme Right Size 13

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
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
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
NOJ PROSTHESIS, BREAST, EXTERNAL, NO ADHESIVE

GMDN Terms

Code Name
35676 External breast prosthesis

Identifiers

Type ID
Primary 00643293000267