FDA UDI Not in Commercial Distribution 🇺🇸 United States

Varithena® Administration Pack

DI: 05060116921175 · Model: Version 1 · BIOCOMPATIBLES UK LTD
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Varithena® Administration Pack
Primary DI
05060116921175
Version / Model
Version 1
Company Name
BIOCOMPATIBLES UK LTD
Labeler DUNS
222870839
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2021-09-29
Public Version Status
Update
Public Device Record Key
11eee6b0-be5e-46c5-8cfc-6a8c8295f7d5
Distribution End Date
2020-10-08

Device Description

The Varithena® administration pack (convenience kit) contents: (1 Varithena Transfer Unit, 3 Silicon-free Syringes, 1 Manometer Tube and 2 Compression pads) . The administration pack is not subject to a 510K as each of the components has clearance as a medical device via a 510K (Syringe and Manometer Tubing) or 510K exempt devices (Compression Pads, Varithena Transfer Unit). The Varithena® administration pack is provided with the Varithena® drug product pack to the customer.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

GMDN Terms

Code Name
41222 Medication transfer set

Identifiers

Type ID
Primary 05060116921175

Customer Contacts

Phone
855 971 8346