FDA.reportPublic FDA data

Adult Curved Sternal Latch Retractor

Primary DI
B040SRLP1
Brand
Adult Curved Sternal Latch Retractor
Company
GENESEE BIOMEDICAL, INC.
Model
SRLP-1
Catalog number
SRLP-1
Device description
Large Patient Curved Sternal Latch Retractor with 2 sets of Blades Suitable for adult patients >90 kg or with BMI of 35 or above
Published
2024-12-04
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
GADRetractor

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GADRetractorGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B040SRLP1PackageHIBCC1Not in Commercial Distribution
B040SRLP10PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Sternum spreaderA self-locking surgical instrument designed to force apart the surgically-split sternum (the breastbone) to permit surgical cardiac intervention within the thoracic cavity. This device will typically have two interchangeable profiled, pivoted blades (self-adjusting their angle as the instrument is opened) at the distal end that hook over the margins of the severed sternum, and a ratchet mechanism along its horizontal bar to adjust the blades, parting the sternum and maintain its set position once it has been set. It is also known as a sternum retractor and is available in various designs and sizes. It is made of high-grade stainless steel. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
800-786-4980contact@geneseebiomedical.com

Regulatory Flags#

DUNS number
939872651
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
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
B040RPS181100Thoracic Port with Obturator 18x110mmRPS-181102026-03-25
B040RPS18500Thoracic Port with Obturator 18x50mmRPS-18502026-03-25
B040RPS18700Thoracic Port with Obturator 18x70mmRPS-18702026-03-25
B040RPS18900Thoracic Port with Obturator 18x90mmRPS-18902026-03-25
B040TF260TransForm McCarthy Annuloplasty RingTF-262024-12-23
B040TF280TransForm McCarthy Annuloplasty RingTF-282024-12-23
B040TF300TransForm McCarthy Annuloplasty RingTF-302024-12-23
B040TF320TransForm McCarthy Annuloplasty RingTF-322024-12-23
B040TF340TransForm McCarthy Annuloplasty RingTF-342024-12-23
B040TF380TransForm McCarthy Annuloplasty RingTF-382024-12-23
B040TF400TransForm McCarthy Annuloplasty RingTF-402024-12-23
B040TF240TransForm McCarthy Annuloplasty RingTF-242024-12-23
B040TF26TransForm McCarthy Annuloplasty RingTF-262024-12-23
B040TF28TransForm McCarthy Annuloplasty RingTF-282024-12-23
B040TF30TransForm McCarthy Annuloplasty RingTF-302024-12-23
B040TF32TransForm McCarthy Annuloplasty RingTF-322024-12-23
B040TF34TransForm McCarthy Annuloplasty RingTF-342024-12-23
B040TF360TransForm McCarthy Annuloplasty RingTF-362024-12-23
B040TF38TransForm McCarthy Annuloplasty RingTF-382024-12-23
B040TF40TransForm McCarthy Annuloplasty RingTF-402024-12-23

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Primary DI, Brand, Company table
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00190776426620MillenniumAvalign Technologies, Inc.GAD2026-08-19
00190776417017MillenniumAvalign Technologies, Inc.GAD2026-08-18
00190776417024MillenniumAvalign Technologies, Inc.GAD2026-08-18
00190776417031MillenniumAvalign Technologies, Inc.GAD2026-08-18
00190776425876MillenniumAvalign Technologies, Inc.GAD2026-08-18
00190776426453MillenniumAvalign Technologies, Inc.GAD2026-08-18
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