FDA UDI In Commercial Distribution 🇺🇸 United States

ViaMed

DI: 00811382010682 · Model: 13312 · RECE INTERNATIONAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
ViaMed
Primary DI
00811382010682
Version / Model
13312
Company Name
RECE INTERNATIONAL CORPORATION
Labeler DUNS
787828537
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2017-05-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
4d45e83d-2308-4979-873f-52723fad19e9

Device Description

Sphygmomanometer Pocket

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Primary 00811382010682
Unit of Use 00811382015663

Premarket Submissions

Submission Number Supplement Number
K043286 000