AccessGUDID - DEVICE: Novo Surgical Inc. (00842331165214)

GUDID

Device Identifier (DI) Information

Brand Name: Novo Surgical Inc.
Version or Model: E8371-23-6
Commercial Distribution Status: In Commercial Distribution
Catalog Number: E8371-23-6
Company Name: NOVO SURGICAL, INC.

Primary DI Number: 00842331165214
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 033029433 *Terms of Use

Device Description: tonsil snare wire, package of 12, 4 1/2"" (11.4 cm), 28 gauge (0.35 mm)

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?
14457	Wire ligature	A sterile, thin metal cord intended to be tied tightly around a blood vessel, the pedicle of a tumour, or other structure in order to constrict it. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
KBZ	Snare, Tonsil

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: 3e3f194c-1f07-4594-8a2a-aac783010977
Public Version Date: November 21, 2022
Public Version Number: 1
DI Record Publish Date: November 13, 2022