2.5mm Drill Bit 180mm 110015

GUDID 00816950028410

2.5mm Drill Bit 180mm

SMV SCIENTIFIC LLC

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Primary Device ID	00816950028410
NIH Device Record Key	ce13e2db-9492-4001-bc5a-48d2a6c44dee
Commercial Distribution Status	In Commercial Distribution
Brand Name	2.5mm Drill Bit 180mm
Version Model Number	110015
Catalog Number	110015
Company DUNS	089645059
Company Name	SMV SCIENTIFIC LLC
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	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

Customer Support Contacts

Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com

Device Dimensions

Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter
Outer Diameter	2.5 Millimeter
Length	180 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816950028410 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K152000

FDA Product Code

HRS	Plate, Fixation, Bone