AccessGUDID - DEVICE: LTV2 (10190752144873)

GUDID

Device Identifier (DI) Information

Brand Name: LTV2
Version or Model: 28767-001
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 28767-001
Company Name: VYAIRE MEDICAL, INC.

Primary DI Number: 10190752144873
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 080456871 *Terms of Use

Device Description: LTV/LTV2 Rolling Stand

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?
42514	Ventilator stand	A mobile device onto which a ventilator (not included) is designed to be mounted/secured so that the ventilator can be safely moved about. It is designed as a floor stand (a vertical pole with a horizontal platform or spars or other form of fastening mechanism) with a set of effectively-spaced wheels to provide mobility and stability.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
CBK	Ventilator, continuous, facility use

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K101643	000

Device Exempt from Premarket Submission: No 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: ca9bf57c-b439-4287-a4f9-c110f904c04e
Public Version Date: March 09, 2021
Public Version Number: 1
DI Record Publish Date: March 01, 2021

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

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: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(833)327-3284
Email: customersupport@vyaire.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES