Tornier Perform

Primary DI
03700386973871
Brand
Tornier Perform
Company
TORNIER
Model
MWE151
Catalog number
MWE151
Device description
CANNULATED REAMER DRIVER
Published
2022-08-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
GFGBIT, SURGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GFGBit, SurgicalGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
03700386973871PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
03700386973871037003869738713700386973871

GMDN Terms#

Term, Definition table
TermDefinition
Surgical screwdriver, reusableA non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+330476613500order@tornier.com

Regulatory Flags#

DUNS number
260324876
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
03700386915260AEQUALISDWB1512015-10-16
03700386916144AEQUALIS REVERSEDDWB9352015-10-16
03700386916151AEQUALIS REVERSEDDWB9362015-10-16
03700386916618AEQUALIS REVERSEDDWD0022015-10-16
03700386916731AEQUALIS REVERSEDDWD0692015-10-16
03700386931529AEQUALIS REVERSED ADAPTERDWD8632015-10-16
03700386931536AEQUALIS REVERSED ADAPTERDWD8642015-10-16
03700386931543AEQUALIS REVERSED ADAPTERDWD8652015-10-16
03700386944871Aequalis™ Ascend™ FlexDWF615B2015-10-16
03700386944888Aequalis™ Ascend™ FlexDWF615C2015-10-16
03700386944895Aequalis™ Ascend™ FlexDWF616A2015-10-16
03700386944901Aequalis™ Ascend™ FlexDWF616B2015-10-16
03700386944918Aequalis™ Ascend™ FlexDWF616C2015-10-16
03700386944925Aequalis™ Ascend™ FlexDWF617A2015-10-16
03700386944932Aequalis™ Ascend™ FlexDWF617B2015-10-16
03700386944949Aequalis™ Ascend™ FlexDWF617C2015-10-16
03700386944956Aequalis™ Ascend™ FlexDWF618A2015-10-16
03700386944963Aequalis™ Ascend™ FlexDWF618B2015-10-16
03700386944970Aequalis™ Ascend™ FlexDWF618C2015-10-16
03700386945045Aequalis™ Ascend™ FlexDWF702A2015-10-16

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