AccessGUDID - DEVICE: Atellica IM aHAVM (00630414301259)

GUDID

Device Identifier (DI) Information

Brand Name: Atellica IM aHAVM
Version or Model: 11207243
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 11207243
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414301259
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: HAV IgM Ab (aHAVM) - Atellica IM - RGT 100T

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?
48283	Hepatitis A virus immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to the Hepatitis A virus in a clinical specimen, using a chemiluminescent immunoassay method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LOL	Hepatitis a test (antibody and igm antibody)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K081716	000
P040018	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
Special Storage Condition, Specify: Store Upright, Protect from Light, Do not freeze, Resuspend.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: c57b66f3-9d26-423a-ba8a-84320e743eec
Public Version Date: November 18, 2021
Public Version Number: 3
DI Record Publish Date: January 15, 2021