Balloon Kyphoplasty Essentials Kit

GUDID 00643169703551

Balloon kyphoplasty kit Balloon kyphoplasty kit

Primary Device ID	00643169703551
NIH Device Record Key	807cc070-05ae-48b1-8a93-b1ac3de4f673
Commercial Distribution Status	In Commercial Distribution
Brand Name	Balloon Kyphoplasty Essentials Kit
Version Model Number	NH103PB-CDS
Company DUNS	830350380
Company Name	MEDTRONIC SOFAMOR DANEK, INC.
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	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Special Storage Condition, Specify	Between 0 and 0 *Store in a Cool Dry Place
Special Storage Condition, Specify	Between 0 and 0 *Store in a Cool Dry Place

Device Issuing Agency	Device ID
GS1	00643169703551 [Primary]

HRX	ARTHROSCOPE

Steralize Prior To Use	false
Device Is Sterile	true

00643169703599	KIT NH152PB-CDS 15/2 SPINE ESSEN FF CDS
00643169703582	KIT NH102PB-CDS 10/2 SPINE ESSEN FF CDS
00643169703575	KIT NH203PB-CDS 20/3 SPINE ESSEN FF CDS
00643169703568	KIT NH153PB-CDS 15/3 SPINE ESSEN FF CDS
00643169703551	KIT NH103PB-CDS 10/3 SPINE ESSEN FF CDS
00643169703544	KIT NH152PB 15/2 SPINE ESSEN FF
00643169703537	KIT NH102PB 10/2 SPINE ESSEN FF
00643169703520	KIT NH203PB 20/3 SPINE ESSEN FF
00643169703513	KIT NH153PB 15/3 SPINE ESSEN FF
00643169703506	KIT NH103PB 10/3 SPINE ESSEN FF