Cyst Puncture Needle without Stylet

GUDID 17350025915569

Vitrolife Sweden AB

Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set Endoscopic cyst-aspiration set

Primary Device ID	17350025915569
NIH Device Record Key	0cb42c3f-dc6b-4214-86f5-18c0838ef956
Commercial Distribution Status	In Commercial Distribution
Brand Name	Cyst Puncture Needle without Stylet
Version Model Number	17804
Company DUNS	631805488
Company Name	Vitrolife Sweden AB
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350025915562 [Primary]
GS1	17350025915569 [Package] Contains: 07350025915562 Package: [5 Units] In Commercial Distribution

FDA Product Code

KNA	Instrument, Manual, Specialized Obstetric-Gynecologic

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	2
Public Version Date	2018-03-29
Device Publish Date	2018-01-09

On-Brand Devices [Cyst Puncture Needle without Stylet]

07350025915616	17810
07350025915593	17807
17350025915569	17804
17350025912414	14814
07350025912370	14810
17350025912346	14807
17350025912315	14804