AccessGUDID - DEVICE: Techno-Aide (G242AGR1059)

GUDID

Device Identifier (DI) Information

Brand Name: Techno-Aide
Version or Model: AGR-105
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AGR-105
Company Name: Techno-Aide, Inc.

Primary DI Number: G242AGR1059
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 843929279 *Terms of Use

Device Description: WALL MOUNTED APRON RACK

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):	No
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?
15928	Safety sign	A device intended to provide visual information on safety warnings, e.g., biological, chemical, radioactive and/or other hazardous or potentially hazardous conditions within a healthcare facility. A sign will typically be manufactured using words, letters, symbols, and/or pictures to convey the information content (e.g., "X-ray in use", "Radiation", "Isolation room", "Pressurized gas"). It is used throughout healthcare facilities to provide visual information on safety to staff, patients, and/or visitors.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EGZ	Holder, film, x-ray

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
No Device Sizes

Device Record Status

Public Device Record Key: 109f1ad7-e46e-4ca3-91d2-eb5c0b10c41e
Public Version Date: February 21, 2023
Public Version Number: 1
DI Record Publish Date: February 13, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
G242AGR10590	1	G242AGR1059		In Commercial Distribution	Package

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(615)350-7030
Email: Customerservice@Techno-Aide.com

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