FDA UDI In Commercial Distribution 🇺🇸 United States

Voyant Maryland Fusion Device with Single-Step Activation

DI: 00607915140809 · Model: EB213 · APPLIED MEDICAL RESOURCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Voyant Maryland Fusion Device with Single-Step Activation
Primary DI
00607915140809
Version / Model
EB213
Company Name
APPLIED MEDICAL RESOURCES CORPORATION
Labeler DUNS
187129135
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-13
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
d0b80589-719f-4ba9-8006-3384b9f750fc

Device Description

Voyant Maryland Fusion Device with Single-Step Activation

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00607915140809
Package 10607915140806

Customer Contacts

Device Sizes

Type Value Unit Text
Shaft Length 44 Centimeter
Outer Diameter 5 Millimeter