FDA.report

Quick Change Spinal Retractor Set

Primary DI
00840199543502
Brand
Quick Change Spinal Retractor Set
Company
KOROS U.S.A., INC.
Model
7314-10
Catalog number
7314-10
Device description
Quick Change Spinal Retractor Set Consists of the Following: 2 x 7314-20, 1 x 7292-40, 1 x 7292-45, 1 x 7292-50, 1 x 7292-55, 1 x 7292-60, 1 x 7292-65, 1 x 7292-70, 1 x 7294-40, 1 x 7294-45, 1 x 7294-50, 1 x 7294-55, 1 x 7294-60, 1 x 7294-65, 1 x 7294-70, 1 x 7316-40, 1 x 7316-45, 1 x 7316-50, 1 x 7316-55, 1 x 7316-60, 1 x 7316-65, 1 x 7316-70, , 1 x 7268-80 & 7314-25
Published
2022-10-31
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

Related Records

Contact Domains

Product Codes

CodeName
GADRetractor

Product Code Classifications

CodeDeviceSpecialtyClass
GADRetractorGeneral, Plastic Surgery1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00840199543502Direct MarkingGS10
10840199543509PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00840199543502008401995435028401995435020840199543502
1084019954350910840199543509

GMDN Terms

TermDefinition
Self-retaining surgical retractor, reusableA hand-operated, self-retaining, one-piece surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not intended to retract the ribs and is not dedicated to ophthalmic surgery, but may otherwise be clinically dedicated. It is designed as a one-piece device (i.e., not a mounting ring, or table-fixed assembly) having two legs with distal hooked blades and a self-retaining mechanism to maintain the legs in an open position for retraction. This is a reusable device.

Device Sizes

TypeValueUnit
Device Size Text, specify0

Storage And Handling

TypeLowHighCondition
Special Storage Condition, Specify00Store in dry place at room temperature

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
1-805-529-0825customerservice@korosUSA.com

Regulatory Flags

DUNS number
007928633
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
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

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