AccessGUDID - DEVICE: Ambler Surgical (00190660175788)

GUDID

Device Identifier (DI) Information

Brand Name: Ambler Surgical
Version or Model: Olivecrona spatula
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 45-456
Company Name: AMBLER SURGICAL CORP.

Primary DI Number: 00190660175788
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 015272206 *Terms of Use

Device Description: Olivecrona spatula, 7'', double-ended, convex, 11.0mm x 13.0mm wide blades, flat 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?
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
HAO	INSTRUMENT, SURGICAL, NON-POWERED

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: ab3c3008-245a-4b2a-90db-b61e5a2620fc
Public Version Date: January 12, 2021
Public Version Number: 1
DI Record Publish Date: January 04, 2021