AccessGUDID - DEVICE: AincA® (B005004690)

GUDID

Device Identifier (DI) Information

Brand Name: AincA®
Version or Model: 00-469
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 00-469
Company Name: ANESTHESIA ASSOCIATES, INC.

Primary DI Number: B005004690
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 002065670 *Terms of Use

Device Description: Stylet, Lighted, Malleable Fiber Optic, Adult (5mm ETT Min), w/Handle (Req 2 AA), ETT Stop, Copper/CPB

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":	Yes
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?
35402	Artificial airway stylet, reusable	A long stiffening wire/rod designed for insertion within the lumen of an artificial airway tube (e.g., endotracheal tube, bronchial tube) to stiffen and/or maintain the shape of the tube to facilitate introduction (intubation). It is designed to be slightly shorter than the tube to avoid damage to the airway during passage, and is withdrawn after intubation has been completed. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BSR	STYLET, TRACHEAL TUBE

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: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Adult

Device Record Status

Public Device Record Key: dd79fe29-1870-48af-a0a4-844e1a74005f
Public Version Date: April 08, 2021
Public Version Number: 1
DI Record Publish Date: March 31, 2021