Healix

Primary DI
00810005662437
Brand
Healix
Company
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Model
CSRW-1000T-401
Device description
Drill 2.5. The HEALIX Compression Screw (HCS) System is indicated for Bone Fractures, Osteotomies, Arthrodesis, Osteochondritis, and Tendon Reattachment. It is intended for, but not limited to, Hand Surgery, Orthopedic Surgery, and Podiatric Surgery but is not intended for attachment or fixation to the posterior elements (pedicles) of the spine.
Published
2019-09-30
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
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HTWBit, Drill

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HTWBit, DrillOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810005662437PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810005662437008100056624378100056624370810005662437

GMDN Terms#

Term, Definition table
TermDefinition
General internal orthopaedic fixation system implantation kitA collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
(210) 545-3713diana@nvisionbiomed.com

Regulatory Flags#

DUNS number
047486041
Device count
1
DM exempt
true
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
00810005667227TrigonWD-1001T-WSLA2025-12-19
00810005668163VertexSTK-1000T-PIN2025-12-18
00810135964180VertexSTK-20-16-162025-12-17
00810135963268ImpactPP-1000T-0322025-09-24
00810135963282ImpactPP-1000T-0422025-09-24
00810135963329ImpactPP-1001T-CUT42025-09-24
00810135963374ImpactPP-1001T-CUT32025-09-24
00810135963404ImpactPP-1000T-DEP342025-09-24
00810135963411ImpactPP-1001T-SLAP2025-09-24
00810135963640ImpactKWIRE-14-127S2025-09-24
00810135963657ImpactINST-1000T-M2502025-09-24
00810135963336ImpactPP-1000T-3012025-09-23
00810135963343ImpactPP-1000T-4012025-09-23
00810135963169ImpactPP-1001T-3002025-09-22
00810135963183ImpactPP-1001T-4002025-09-22
00810135963251ImpactPP-1000T-3002025-09-22
00810135963275ImpactPP-1000T-4002025-09-22
00810135963381ImpactPP-1000T-2002025-09-22
00810135963619ImpactPP-30-502025-09-22
00810135963626ImpactPP-40-502025-09-22

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Primary DI, Brand, Company table
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