SafeSept RF Transseptal Guidewire

GUDID 30858769006525

Cardiac transseptal needle, single-use

Primary Device ID	30858769006525
NIH Device Record Key	5890b0f7-f0a6-41f3-8b98-24c61818a562
Commercial Distribution Status	In Commercial Distribution
Brand Name	SafeSept RF Transseptal Guidewire
Version Model Number	SSRF135
Company DUNS	081047841
Company Name	PPMDM
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00858769006524 [Primary]
GS1	30858769006525 [Package] Contains: 00858769006524 Package: Box [5 Units] In Commercial Distribution

DXF	Catheter, Septostomy

Steralize Prior To Use	false
Device Is Sterile	true

30858769006556	0.035" x 230cm x Retention Transseptal Wires in Five Unit Box
30858769006549	0.035" x 230cm x J-Curve Transseptal Wires in Five Unit Box
30858769006532	0.035" x 180cm x Retention Transseptal Wires in Five Unit Box
30858769006525	0.035" x 180cm x J-Curve Transseptal Wires in Five Unit Box
00858769006517	0.032" x 230cm x Retention Transseptal Wires in Five Unit Box
30858769006501	0.032" x 230cm x J-Curve Transseptal Wires in Five Unit Box
00858769006494	0.032" x 180cm x Retention Transseptal Wires in Five Unit Box
30858769006488	0.032" x 180cm x J-Curve Transseptal Wires in Five Unit Box