AccessGUDID - DEVICE: Black Belt Cervical Retractor Basic Set (10840199501769)

GUDID

Device Identifier (DI) Information

Brand Name: Black Belt Cervical Retractor Basic Set
Version or Model: 7320-00
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 7320-00
Company Name: KOROS U.S.A., INC.

Primary DI Number: 10840199501769
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 007928633 *Terms of Use

Device Description: Black Belt Cervical Retractor Basic Set, Consists of the Following: Black Finish Stainless Steel Frames and Blades. 1x 7320-22 - Korpectomy Retractor frame Right 1x 7320-20 - Retractor frame Left 1x 7320-30 - Retractor frame Offset 2x 7320-40 - Blade Inserting Clamps 2x 7322-34 - Pronged Blade 34mm, 2x 7322-40 - Pronged Blade 40mm, 2x 7322-45 - Pronged Blade 45mm, 2x 7322-50 - Pronged Blade 50mm, 2x 7322-55 - Pronged Blade 55mm, 2x 7322-60 - Pronged Blade 60mm, 2x 7322-70 - Pronged Blade 70mm, 2x 7324-34 - Blunt Blade 34mm, 2x 7324-40 - Blunt Blade 40mm, 2x 7324-45 - Blunt Blade 45mm, 2x 7324-50 - Blunt Blade 50mm, 2x 7324-55 - Blunt Blade 55mm, 2x 7324-60 - Blunt Blade 60mm, 2x 7324-70 - Blunt Blade 70mm, 4x 7326-40 - Two-Level Blade Pronged 40mm, 4x 7326-47 - Two-Level Blade Pronged 47mm, 4x 7326-55 - Two-Level Blade Pronged 55mm, 2x 7328-40 - Two-Level Blade Blunt 40mm, 2x 7328-47 - Two-Level Blade Blunt 47mm, 2x 7328-55 - Two-Level Blade Blunt 55mm, 1x 7320-90 - Sterilizing Instrument Case with silicone pads

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
45182	Self-retaining surgical retractor, reusable	A 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.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GZT	Retractor, Self-Retaining, For Neurosurgery

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K935529	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store in dry place at room temperature

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: c6aadf06-823f-4d38-918c-0173f426a648
Public Version Date: July 06, 2021
Public Version Number: 1
DI Record Publish Date: June 28, 2021