AccessGUDID - DEVICE: HNM Medical (00842962114513)

GUDID

Device Identifier (DI) Information

Brand Name: HNM Medical
Version or Model: HNM-1-23-7106
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HNM-1-23-7106
Company Name: HNM STAINLESS, LLC.

Primary DI Number: 00842962114513
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 806754185 *Terms of Use

Device Description: HARRINGTON PEMBERTON RETRACTOR, 12 1/2", 2 1/2"X7" BLADES

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:	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?
36293	Abdominal/intestinal spatula	A hand-held manual surgical instrument designed to manipulate the intestines and organs of the abdomen during a surgical intervention in the abdominal cavity. It typically consists of a large, flat, blunt blade (no sharp edges) at the distal end and a strong handle at the proximal end. It is usually made of high-grade stainless steel and is available with a variety of blade designs (e.g., curved and flat or straight and flat with a rounded end, or right-angled); some blade types may have a serrated surface to help retain the slippery abdominal tissues. The handle is typically designed to provide a non-slip grip. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GAD	Retractor

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: 539e7da8-66c6-498c-9e54-ca5040e37f74
Public Version Date: February 14, 2023
Public Version Number: 1
DI Record Publish Date: February 06, 2023