AccessGUDID - DEVICE: Atellica CH LIDO (00630414220680)

GUDID

Device Identifier (DI) Information

Brand Name: Atellica CH LIDO
Version or Model: 11097539
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 11097539
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414220680
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: Lidocaine (LIDO) Atellica CH - RGT 200T

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?
61894	Lidocaine therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry	A collection of reagents and other associated materials intended to be used for the quantitative measurement and therapeutic monitoring of the cardiovascular drug lidocaine in a clinical specimen, using a nephelometry/turbidimetry method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KLR	ENZYME IMMUNOASSAY, LIDOCAINE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K033809	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
Special Storage Condition, Specify: Store Upright; Do not freeze
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 309fd27a-9974-4a30-b1f8-5bf5c8033478
Public Version Date: November 18, 2021
Public Version Number: 3
DI Record Publish Date: October 08, 2018