Primus

Primary DI
00840606174800
Brand
Primus
Company
SPINAL ELEMENTS, INC.
Model
66440-000
Device description
K-WIRE HOLDER
Published
2026-03-06
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
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840606174800PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840606174800008406061748008406061748000840606174800

GMDN Terms#

Term, Definition table
TermDefinition
Wire holding/twisting forcepsA surgical instrument with specially designed sturdy blades used to grip, tighten and/or twist wires that are being applied to the patient during a surgical intervention. It typically has a scissors-like design with ring handles, is made of high-grade stainless steel and may be self-retaining. It is available in various sizes and the working end can have a variety of jaw designs, e.g., typically short and broad with carbide inserts, but some may be long with side protruding posts around which the loose end of the wire are secured to provide greater grip. The blades/handles are typically strong in profile. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
7606070121customerservice@spinalelements.com

Regulatory Flags#

DUNS number
610712213
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
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840606197007MERCURY61085-003-012026-10-16
00840606197014MERCURY61085-003-022026-10-16
00840606197021MERCURY61085-004-012026-10-16
00840606197038MERCURY61085-004-022026-10-16
00840606104074Hero01001-0012015-07-08
00840606104081Hero01001-0022015-07-08
00840606104098Hero01001-0052015-07-08
00840606104104Hero01001-0102015-07-08
00840606104111Hero01002-0012015-07-08
00840606104128Hero01002-0032015-07-08
00840606104135Hero01002-0082015-07-08
00840606104142Hero01003-0012015-07-08
00840606104159Hero01003-0052015-07-08
00840606104166Hero01003-0102015-07-08
00840606104173Hero01004-0052015-07-08
00840606104180Hero01004-0102015-07-08
00840606191425Primus66580-0012026-09-30
00840606191432Primus66580-0022026-09-30
00840606191449Primus66581-0102026-09-30
00840606191456Primus66581-0122026-09-30

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10840642149838Proficient® Posterior Cervical Spine SystemSpine Wave, Inc.LXH2026-10-20
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B504OMBR9505023020BrasselerProvisionLXH2026-10-20
B504OMBR9505023030BrasselerProvisionLXH2026-10-20
B504OMDP86011710BrasselerProvisionLXH2026-10-20
B504OMST60070031000BrasselerProvisionLXH2026-10-20
B504OMST60070031500BrasselerProvisionLXH2026-10-20
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B504OMZB005901020000BrasselerProvisionLXH2026-10-20
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00810161900305EARP, TRIAL 22X35X12 6°RETROPSOAS TECHNOLOGIES, LLCLXH2026-10-16
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00810161900329EARP, TRIAL 22X35X12 12°RETROPSOAS TECHNOLOGIES, LLCLXH2026-10-16
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00810161901418EARP TRIAL 22x40x10 6°RETROPSOAS TECHNOLOGIES, LLCLXH2026-10-16
00810161901425EARP TRIAL 22x40x12 6°RETROPSOAS TECHNOLOGIES, LLCLXH2026-10-16