AccessGUDID - DEVICE: HNM MEDICAL (00842962104972)

GUDID

Device Identifier (DI) Information

Brand Name: HNM MEDICAL
Version or Model: HNM-e-2CD
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HNM-e-2CD
Company Name: HNM STAINLESS, LLC.

Primary DI Number: 00842962104972
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 806754185 *Terms of Use

Device Description: ETHOS WIRE, TAPER POINT, (2) MO-6 26mm, 1/2 CIRCLE, #2 SUTURE, 36", WHITE/BLUE, 12/PK

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":	Yes
For Single-Use:	No
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?
46599	Pylorus clamp	A hand-held manual surgical instrument intended for atraumatic compression of the pylorus (the lower muscular opening of the stomach) during a surgical procedure. It is typically made of high-grade stainless steel, is available in various sizes, and has a robust design, e.g., the working end will have strong blades that are flat and broad in profile so that they do not cause trauma to duodenal tissue. The blades are serrated with parallel grooves and/or serrations to provide grip and the handle is also robust to allow the required pressure to be applied by the surgeon. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEN	Forceps, General & Plastic Surgery

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: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: 577078cd-e3d0-4eaa-a923-40bfa5ee07d9
Public Version Date: June 05, 2023
Public Version Number: 1
DI Record Publish Date: May 27, 2023