AccessGUDID - DEVICE: LiNA OperaScope™ Biopsy Forceps (05708265012442)

GUDID

Device Identifier (DI) Information

Brand Name: LiNA OperaScope™ Biopsy Forceps
Version or Model: OP-FCP-6
Commercial Distribution Status: In Commercial Distribution
Catalog Number: OP-FCP-6
Company Name: Lina Medical ApS

Primary DI Number: 05708265012442
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 305088619 *Terms of Use

Device Description: Alligator Biopsy Forceps for hysteroscopy and cystoscopy. Minimum channel diameter: Ø2.0mm.

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?
46228	Rigid endoscopic biopsy forceps, single-use	A rigid, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., laparoscopy, thoracoscopy, spinoscopy, arthroscopy). It is typically constructed as a long instrument with one sliding and one stationary rod whose distal ends are equipped with scissors-like cups with cutting edge rims, which are operated by a control handle at the proximal end of the instrument. It is introduced into the body through an artificial orifice of the body or the working channel of the endoscope. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HTD	Forceps

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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: aad1d96a-b70a-4d4d-a8d7-ba9de9ed49cf
Public Version Date: December 16, 2024
Public Version Number: 3
DI Record Publish Date: August 03, 2020