FDA.reportPublic FDA data

N/A

Primary DI
B089B61121TT0
Brand
N/A
Company
BLACK & BLACK SURGICAL, INC.
Model
B61121-TT
Catalog number
B61121-TT
Device description
LUMIVIEW "MIDI" RETRACTOR BLADE; 1 1/4"(30MM) X 5 3/8"(13.5CM), WITH SERRATIONS AND TEETH
Published
2022-09-12
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
FDGRETRACTOR, FIBEROPTIC

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FDGRetractor, FiberopticGastroenterology, Urology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B089B61121TT0PrimaryHIBCC0

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

Contacts#

Phone, Email table
PhoneEmail
+1(770)414-4880info@blackandblacksurgical.com

Regulatory Flags#

DUNS number
004382282
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
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
00840329811518N/AB79808B798082022-09-21
00840329811525N/AB79809B798092022-09-21
B089B784600Headlight CableB78460B784602016-07-29
B089B784640Headlight CableB78464B784642016-07-29
B089B797180Fiberoptic Cable B79718B797182016-07-29
B089B797190Fiberoptic Cable B79719B797192016-07-29
B089B797220Fiberoptic Cable B79722B797222016-07-29
B089B797230Fiberoptic Cable B79723B797232016-07-29
B089B797240Fiberoptic Cable B79724B797242016-07-29
B089B797250Fiberoptic Cable B79725B797252016-07-29
B089B797260Fiberoptic Cable B79726B797262016-07-29
B089B797270Fiberoptic Cable B79727B797272016-07-29
B089B797280Fiberoptic Cable B79728B797282016-07-29
B089B797590Fiberoptic Cable B79759B797592016-07-29
B089B797600Fiberoptic Cable B79760B797602016-07-29
B089B797610Fiberoptic Cable B79761B797612016-07-29
B089B797650Fiberoptic Cable B79765B797652016-07-29
B089B797660Fiberoptic Cable B79766B797662016-07-29
B089B797670Fiberoptic Cable B79767B797672016-07-29
B089B797680Fiberoptic Cable B79768B797682016-07-29

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00840183525620BR Surgical, LLCBR Surgical, LLCFDG2024-03-04
00888515319363BOSS InstrumentsBOSS INSTRUMENTS, LTD., INC.FDG2024-02-21
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