FDA UDI In Commercial Distribution 🇺🇸 United States

ViaMed

DI: 00811382019647 · Model: 17312-Y · RECE INTERNATIONAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
32

Basic Information

Brand Name
ViaMed
Primary DI
00811382019647
Version / Model
17312-Y
Company Name
RECE INTERNATIONAL CORPORATION
Labeler DUNS
787828537
Distribution Status
In Commercial Distribution
Device Count in Pkg
32
Record Status
Published
Publish Date
2017-09-20
Public Version
4
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
bd757ce7-563d-4bb8-8414-90d515427dec

Device Description

Sharp Container 5liter Yellow

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MMK Container, Sharps

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Primary 00811382019647
Unit of Use 00811382018060

Premarket Submissions

Submission Number Supplement Number
K082042 000