AccessGUDID - DEVICE: Ambler Surgical (00190660054410)

GUDID

Device Identifier (DI) Information

Brand Name: Ambler Surgical
Version or Model: Glassman stomach/intestinal forceps
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 30-675
Company Name: AMBLER SURGICAL CORP.

Primary DI Number: 00190660054410
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 015272206 *Terms of Use

Device Description: Glassman stomach/intestinal forceps, 9 1/2'', straight, 2 1/2'' long atraumatic serrated jaws, ring handle

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):	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?
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
KOA	SURGICAL INSTRUMENTS, G-U, MANUAL (AND ACCESSORIES)

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: 29a8a77a-35cc-403a-b308-05a8ca5e89c5
Public Version Date: January 15, 2021
Public Version Number: 1
DI Record Publish Date: January 07, 2021