FDA UDI In Commercial Distribution 🇺🇸 United States

ViaMed

DI: 00811382015595 · Model: 13013 · RECE INTERNATIONAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
ViaMed
Primary DI
00811382015595
Version / Model
13013
Company Name
RECE INTERNATIONAL CORPORATION
Labeler DUNS
787828537
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-09-22
Public Version
1
Public Version Date
2020-09-30
Public Version Status
New
Public Device Record Key
7e8a426a-1f79-4fd5-a8ea-7dae160e2f00

Device Description

Polyethylene and stainless steel. Fine gauge, tri-bevel tip for virtually painless smapling. Universal Design. Fits almost all lancing devices.

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 00811382010606
Primary 00811382015595
Unit of Use 00811382010750

Customer Contacts

Phone
3053626555