AccessGUDID - DEVICE: Precisor (30653405052054)

GUDID

Device Identifier (DI) Information

Brand Name: Precisor
Version or Model: 000823
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 000823
Company Name: Conmed Corporation

Primary DI Number: 30653405052054
Issuing Agency: GS1
Commercial Distribution End Date: June 06, 2022
Device Count: 10
Labeler D-U-N-S® Number*: 071595540 *Terms of Use

Device Description: Precisor Jumbo Disposable Biopsy Forceps

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?
11775	Open-surgery biopsy forceps, reusable	A hand-held manual surgical instrument designed to obtain soft-tissue biopsy specimens from an open surgical wound or from within/near a large natural orifice (e.g., vagina, rectum) for histopathological examination; it is not intended for endoscopic or catheterized access. It is a metallic forceps-like instrument with a distal mechanism designed to bite/punch the biopsy sample and hold it for extraction when the handles are squeezed together. It is not designed for cutting bone (i.e., not a rongeur). This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FCL	FORCEPS, BIOPSY, NON-ELECTRIC

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: Yes

Sterilization Method [?]
Ethylene Oxide

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Depth: 3.8 Millimeter
Length: 230 Centimeter
Width: 3.1 Millimeter

Device Record Status

Public Device Record Key: 4f6e3f3b-c925-40b7-9ca6-e1c2841e18ca
Public Version Date: June 07, 2022
Public Version Number: 2
DI Record Publish Date: November 28, 2020