FDA UDI In Commercial Distribution 🇺🇸 United States

Trinity Sterile, Inc.

DI: 10841767104870 · Model: 80359 · Trinity Sterile, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Trinity Sterile, Inc.
Primary DI
10841767104870
Version / Model
80359
Company Name
Trinity Sterile, Inc.
Labeler DUNS
154424043
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-30
Public Version
2
Public Version Date
2023-12-13
Public Version Status
Update
Public Device Record Key
014e8e0d-1478-4459-85a5-125e9e25130e

Device Description

SUTURE REMOVAL TRAY

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MCZ Suture removal kit

GMDN Terms

Code Name
13894 Suture removal kit

Identifiers

Type ID
Package 00841767104873
Primary 10841767104870