AccessGUDID - DEVICE: SUSI (04046963892784)

GUDID

Device Identifier (DI) Information

Brand Name: SUSI
Version or Model: BM226SU
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: BM226SU
Company Name: Aesculap AG

Primary DI Number: 04046963892784
Issuing Agency: GS1
Commercial Distribution End Date: October 26, 2021
Device Count: 20
Labeler D-U-N-S® Number*: 315018218 *Terms of Use

Device Description: CRILE-WOOD SUSI Needleholder, 8", (200 mm), sterile, disposable, pack of 20 pcs, single packed

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:	Yes
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?
47568	Suturing needle holder, single-use	A hand-held manual surgical instrument designed to grasp a suture needle when pushing/pulling the needle and attached suture through tissue during suturing. It has short serrated jaws at the distal end to provide better grip of the needle, and is available in a wide variety of sizes and designs, such as: 1) a self-retaining, scissors-like design with ring handles at the proximal end; 2) a tweezers-like design with bowed, hinged handles that are operated by squeezing them together; and 3) a heavy-duty pincer-like design. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HXK	HOLDER, NEEDLE; ORTHOPEDIC

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: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

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: 933f6420-54a5-4997-bd9b-5e741ab65b26
Public Version Date: January 19, 2022
Public Version Number: 3
DI Record Publish Date: April 24, 2020