AccessGUDID - DEVICE: Grasper Atraumatic Shaft insert 33cm Disposable (B354OS335MGI0)

GUDID

Device Identifier (DI) Information

Brand Name: Grasper Atraumatic Shaft insert 33cm Disposable
Version or Model: OS335MGI
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: ORANGE SURGICAL INSTRUMENTS, LLC

Primary DI Number: B354OS335MGI0
Issuing Agency: HIBCC
Commercial Distribution End Date: July 01, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 047063695 *Terms of Use

Device Description: Grasper Atraumatic Shaft insert 33cm Disposable

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:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
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?
61875	Endoscopic electrosurgical electrode, monopolar, single-use	A sterile, invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a monopolar configuration (i.e., used with a patient contact return electrode) to tissues for cutting/coagulation/ablation during endoscopic (e.g., laparoscopic, arthroscopic) surgery. It is available in a variety of forms (e.g., exchangeable electrode for electrosurgical forceps, rigid electrode, flexible endoscopic probe) which may include a lumen for suction/irrigation. It does not include a handpiece or housing and has no electrical or mechanical controls (e.g., does not include ring-handles); it is not intended for gas-enhanced electrosurgery. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	Electrosurgical, Cutting & Coagulation & Accessories

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K101733	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 9d8c0a80-55ef-432a-9ba8-88185d3bbe35
Public Version Date: January 01, 2024
Public Version Number: 7
DI Record Publish Date: November 07, 2016