Lattus

Primary DI
00843059127232
Brand
Lattus
Company
TEDAN SURGICAL INNOVATIONS, L.L.C.
Model
LAT-4100
Device description
Duet 22 Split Tube Blade Pair, 100MM
Published
2026-07-20
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
MDMInstrument, Manual, Surgical, General Use

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MDMInstrument, Manual, Surgical, General UseGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00843059127232PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00843059127232008430591272328430591272320843059127232

GMDN Terms#

Term, Definition table
TermDefinition
Surgical retractor/retraction system blade, reusableA distal component of a surgical retraction system, surgical retractor, and/or surgical instrument assist arm system designed to function as a parting edge to separate the margins of a wound/incision during a surgical procedure. It is intended to be attached to the frame (e.g., mounting ring/bar) of a surgical retraction system, or may be fixed onto a retractor handle; it does not include a handle. It is a metal device, sometimes referred to as a variable or vario retractor blade when assembled with a separate retractor handle, because it is available in a variety of lengths and sizes. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
791619393
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
00843059127188LattusLAT-20062026-07-20
00843059127195LattusLAT-20072026-07-20
00843059127201LattusLAT-21202026-07-20
00843059127218LattusLAT-31202026-07-20
00843059127225LattusLAT-40902026-07-20
00843059127249LattusLAT-41102026-07-20
00843059127256LattusLAT-41202026-07-20
00843059127263LattusLAT-41302026-07-20
00843059127270LattusLAT-41402026-07-20
00843059127287LattusLAT-41502026-07-20
00843059127294LattusLAT-41602026-07-20
00843059127300LattusLAT-41702026-07-20
00843059127317LattusLAT-41802026-07-20
00843059127331LattusLAT-15632026-07-20
00843059127348LattusLAT-15312026-07-20
00843059127355LattusLAT-15322026-07-20
00843059127379LattusLAT-15042026-07-20
00843059127386LattusLAT-05142026-07-20
00843059127393LattusLAT-15152026-07-20
00843059127416LattusLAT-15272026-07-20

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00888867574519Arthrex®ARTHREX, INC.MDM2026-09-18
00888867574526Arthrex®ARTHREX, INC.MDM2026-09-18
00888867574533Arthrex®ARTHREX, INC.MDM2026-09-18
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10888277688902MEDLINEMEDLINE INDUSTRIES, INC.MDM2026-09-18
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10888277688964MEDLINEMEDLINE INDUSTRIES, INC.MDM2026-09-18
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10080196321384MEDLINEMEDLINE INDUSTRIES, INC.MDM2026-09-14
10888277688995MEDLINEMEDLINE INDUSTRIES, INC.MDM2026-09-14
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10080196320417MEDLINEMEDLINE INDUSTRIES, INC.MDM2026-09-09