FDA UDI In Commercial Distribution 🇺🇸 United States

Trinity Sterile, Inc.

DI: 10841767106751 · Model: 85162 · Trinity Sterile, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Trinity Sterile, Inc.
Primary DI
10841767106751
Version / Model
85162
Company Name
Trinity Sterile, Inc.
Labeler DUNS
154424043
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-04
Public Version
2
Public Version Date
2023-10-24
Public Version Status
Update
Public Device Record Key
8da068d6-c016-447e-8ccb-069e2dc0cc09

Device Description

I&D 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
Moist Heat or Steam Sterilization

Product Codes

Code Name
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
35118 Incision/drainage kit

Identifiers

Type ID
Package 00841767106754
Primary 10841767106751