AccessGUDID - DEVICE: VITROS (10758750000661)

GUDID

Device Identifier (DI) Information

Brand Name: VITROS
Version or Model: 6800336
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 6800336
Company Name: ORTHO CLINICAL DIAGNOSTICS

Primary DI Number: 10758750000661
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 215865786 *Terms of Use

Device Description: VITROS Immunodiagnostic Products NTx Controls

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):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
47420	Collagen type I cross-linked C-telopeptide IVD, kit, chemiluminescent immunoassay	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of collagen type I cross-linked C-telopeptides and/or metabolites [e.g., beta-isomerized C-terminal telopeptide of type I collagen (beta-CTx)] in a clinical specimen, using a chemiluminescent immunoassay method. Collagen type I cross-linked C-telopeptide and metabolites are typically used to aid in the diagnosis of conditions associated with elevated bone lysis/resorption (e.g., multiple myeloma, osteolytic metastasis, osteoporosis, rheumatoid arthritis).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JJX	Single (specified) analyte controls (assayed and unassayed)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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: May be stored frozen, avoid repeated freeze-thaw cycles
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: c197cb73-b9cc-450b-a891-1a2efbb417f1
Public Version Date: June 21, 2023
Public Version Number: 3
DI Record Publish Date: April 08, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20758750000668	30	10758750000661		In Commercial Distribution	Case

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

Customer Contact

[?]

No Customer Contact currently defined

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