AccessGUDID - DEVICE: Adson Forceps tissue 1x2 teeth 12,5cm (G2021503024120)

GUDID

Device Identifier (DI) Information

Brand Name: Adson Forceps tissue 1x2 teeth 12,5cm
Version or Model: 150302412
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 15-03024-12
Company Name: CONCISE ENTERPRISES

Primary DI Number: G2021503024120
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 645816062 *Terms of Use

Device Description: Adson forceps are surgical instruments used for grasping and manipulating delicate tissues during surgical procedures, with 1x2 teeth and a length of 12.5cm. The teeth provide a secure grip, while the slim profile allows for precise control.

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):	No
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?
62489	Dressing/utility forceps, tweezers-like, single-use	A hand-held manual instrument designed primarily for non-dedicated grasping of devices, sponges and/or dressings during a procedure; it is not intended for endoscopic use. It typically has a tweezers-like design with two blades joined at the proximal (non-working) end with variously designed tips at the working end. It is made of metal and/or plastic materials and is available in various sizes. 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: a384b238-ef8d-4a03-b579-5c8c5b541815
Public Version Date: June 02, 2023
Public Version Number: 2
DI Record Publish Date: April 15, 2023