FDA UDI In Commercial Distribution 🇺🇸 United States

i-port ADVANCE™

DI: 05705244014213 · Model: MMT-100 · Unomedical A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
i-port ADVANCE™
Primary DI
05705244014213
Version / Model
MMT-100
Company Name
Unomedical A/S
Labeler DUNS
306032491
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-03-31
Public Version
4
Public Version Date
2021-04-12
Public Version Status
Update
Public Device Record Key
18608c20-7e2f-47ee-a066-0536bba07abd

Device Description

Single use injection port for subcutaneous injection. The injection port must be used as described in the Instruction for Use.

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days

GMDN Terms

Code Name
17180 Subcutaneous infusion/injection port needle

Identifiers

Type ID
Package 05705244014220
Primary 05705244014213
Unit of Use 05705244014237

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 90 degree
Depth 6 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature. Do not store or leave the device in direct sunlight