Vertebroplasty Needle

GUDID 08053175016125

Vertebral bone biopsy procedure kit, single-use

Primary Device ID	08053175016125
NIH Device Record Key	bb4a3b94-9614-45e5-9dc9-723e526d9558
Commercial Distribution Status	In Commercial Distribution
Brand Name	Vertebroplasty Needle
Version Model Number	49632
Company DUNS	437941789
Company Name	ADRIA SRL
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	true
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 Issuing Agency	Device ID
GS1	08053175016125 [Primary]

OCJ	Spinal Channeling Instrument, Vertebroplasty

Steralize Prior To Use	true
Device Is Sterile	true

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

[08053175016125]

Ethylene Oxide

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