FDA UDI In Commercial Distribution 🇺🇸 United States

Follicle Aspiration Set Reduced Single Lumen, Luer

DI: 07350025915487 · Model: 17180 · Vitrolife Sweden AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Follicle Aspiration Set Reduced Single Lumen, Luer
Primary DI
07350025915487
Version / Model
17180
Company Name
Vitrolife Sweden AB
Labeler DUNS
631805488
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-26
Public Version
1
Public Version Date
2024-12-04
Public Version Status
New
Public Device Record Key
7957320a-7192-4ad8-9101-f95774999ce1

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
MQE Needle, Assisted Reproduction

GMDN Terms

Code Name
45676 IVF oocyte aspiration needle, single-use

Identifiers

Type ID
Package 17350025915484
Primary 07350025915487