FDA UDI In Commercial Distribution 🇺🇸 United States

Vitalitec

DI: 04250325494688 · Model: VK.J804QRF · Vitalitec International Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitalitec
Primary DI
04250325494688
Version / Model
VK.J804QRF
Catalog Number
VK.J804QRF
Company Name
Vitalitec International Medizintechnik GmbH
Labeler DUNS
328485453
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-28
Public Version
1
Public Version Date
2023-07-06
Public Version Status
New
Public Device Record Key
a7f6d0cb-44d5-45c7-8295-ef71540d18ff

Device Description

QUICK RELEASE Micro Kerrison Rongeur, thin footplate, 12 mm bite opening, 40d UP, 4mm, 8", serated handle

Device Characteristics

Single Use
No
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
MR Unsafe
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
HAE RONGEUR, MANUAL

GMDN Terms

Code Name
35541 Spinal rongeur

Identifiers

Type ID
Primary 04250325494688