AccessGUDID - DEVICE: HNM Medical (00842962124208)

GUDID

Device Identifier (DI) Information

Brand Name: HNM Medical
Version or Model: HNM-1-50-9741
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HNM-1-50-9741
Company Name: HNM STAINLESS, LLC.

Primary DI Number: 00842962124208
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 806754185 *Terms of Use

Device Description: RECTAL SNARE, 15 3/4"

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?
32098	Laparotomy ring	A surgical instrument designed in the shape of a circular band that is set into the abdominal wall to hold open an incision during surgery on the abdominal organs. It functions as a fixed-length access retractor or wound retractor and is used in procedures where entry of the surgeon's hand into the abdominal cavity may facilitate the procedure, and for the extraction of large specimens. This device is used in colorectal, urological, gynaecological, and general surgical procedures. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FGX	Snare, Non-Electrical

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: 49ae8877-f882-4caa-b620-0fc83c48912a
Public Version Date: April 25, 2023
Public Version Number: 1
DI Record Publish Date: April 17, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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