Trinica® Select

Primary DI
00889024323827
Brand
Trinica® Select
Company
ZIMMER SPINE, INC.
Model
07.00784.001
Catalog number
07.00784.001
Published
2016-06-22
Public version status
Update
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
KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024323827PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024323827008890243238278890243238270889024323827

GMDN Terms#

Term, Definition table
TermDefinition
Surgical drill guide, reusableA hand-held tubular surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone), and to protect the surrounding soft tissue while the drill is in operation. It may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle at its proximal end for holding and manipulation, or it may be held by another device (e.g., orthopaedic jig). The device is typically dedicated to drill bit size, made of metal, and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(866)774-6368zimmer.consumerrelations@zimmerbiomet.com

Regulatory Flags#

DUNS number
787663400
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889024333499Minit®300-4018300-40182015-09-24
00889024334977Sequoia®3306-55503306-55502015-09-24
00889024335004Sequoia®3306-65303306-65302015-09-24
00889024335059Sequoia®3306-65553306-65552015-09-24
00889024335134Sequoia®3306-75603306-75602015-09-24
00889024335165Sequoia®3306-85403306-85402015-09-24
00889024335486Sequoia®3361-0553361-0552016-06-23
00889024331419InFix® Anterior Lumbar System1850-51121850-51122016-06-23
00889024331426InFix® Anterior Lumbar System1850-51141850-51142016-06-23
00889024331433InFix® Anterior Lumbar System1850-53081850-53082016-06-23
00889024331440InFix® Anterior Lumbar System1850-53141850-53142016-06-23
00889024331457InFix® Anterior Lumbar System1850-55081850-55082016-06-23
00889024331464InFix® Anterior Lumbar System1850-55121850-55122016-06-23
00889024402577InFix® Anterior Lumbar System1850-51001850-51002016-06-23
00889024402584InFix® Anterior Lumbar System1850-51081850-51082016-06-23
00889024402591InFix® Anterior Lumbar System1850-51101850-51102016-06-23
00889024402607InFix® Anterior Lumbar System1850-53101850-53102016-06-23
00889024402614InFix® Anterior Lumbar System1850-53121850-53122016-06-23
00889024402621InFix® Anterior Lumbar System1850-55101850-55102016-06-23
00889024402638InFix® Anterior Lumbar System1850-55141850-55142016-06-23

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Primary DI, Brand, Company table
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00840283402203VyPlate™VY SPINE LLCKWQ2026-03-19
08800071055440ASTEROSTEONIC CO.,Ltd.KWQ2026-03-19
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