FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 16973881680153 · Model: 1010-C · Tianjin Newtrans Technology Development
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
N/A
Primary DI
16973881680153
Version / Model
1010-C
Company Name
Tianjin Newtrans Technology Development
Labeler DUNS
527173399
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-03-03
Public Version
1
Public Version Date
2023-03-13
Public Version Status
New
Public Device Record Key
41f3afb1-3070-4623-88c1-20866c1b2e84

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
63649 General-purpose surgical suction system, vacuum

Identifiers

Type ID
Package 26973881680143
Primary 16973881680153
Unit of Use 06973881680149