AccessGUDID - DEVICE: SPIROTRAC (65099169688003)

GUDID

Device Identifier (DI) Information

Brand Name: SPIROTRAC
Version or Model: 7000
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: VITALOGRAPH (IRELAND) LIMITED

Primary DI Number: 65099169688003
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 219683489 *Terms of Use

Device Description: 7000 SPIROTRAC

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?
64339	Cardiopulmonary parameter spot-check measurement software	An application software program intended to be installed on a computer/workstation to assist a healthcare provider in the spot-check (user-initiated) measurement of a cardiovascular and/or pulmonary parameter(s) [e.g., blood pressure, electrocardiography (ECG), respiratory rate, haemoglobin oxygen saturation (SpO2)]; it might also be intended for additional physiological measurements [e.g., electromyography (EMG), galvanic skin response (GSR)]. It is intended to display, store, and allow communication of the physiological data, and may include interpretive algorithms to assist diagnosis; it is not intended for continuous bedside/intraoperative monitoring.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
BZG	SPIROMETER, DIAGNOSTIC

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K141546	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: 57d7f0d5-d820-4e4e-a541-d46c0fdebcdd
Public Version Date: February 05, 2024
Public Version Number: 3
DI Record Publish Date: April 30, 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
05099169688001	1	65099169688003		In Commercial Distribution

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

Customer Contact

[?]

No Customer Contact currently defined

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