AccessGUDID - DEVICE: Dimension® Flex® reagent cartridge PCHE (00842768014178)

GUDID

Device Identifier (DI) Information

Brand Name: Dimension® Flex® reagent cartridge PCHE
Version or Model: 10444964
Commercial Distribution Status: In Commercial Distribution
Catalog Number: DF51
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00842768014178
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 4
Labeler D-U-N-S® Number*: 005088112 *Terms of Use

Device Description: Pseudocholinesterase Flex® reagent cartridge, 120 tests

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?
52971	Pseudocholinesterase IVD, kit, spectrophotometry	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of the enzyme pseudocholinesterase in a clinical specimen, using a spectrophotometry method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DLI	Acetylcholine chloride, specific reagent for pseudo cholinesterase
DIH	Colorimetry, cholinesterase

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K950180	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
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: 99de8330-4090-4c08-85a4-5bfe851e1d84
Public Version Date: July 06, 2023
Public Version Number: 3
DI Record Publish Date: September 24, 2020