AccessGUDID - DEVICE: RealTime (00884999036130)

GUDID

Device Identifier (DI) Information

Brand Name: RealTime
Version or Model: 08L21-90
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 08L21-90
Company Name: ABBOTT MOLECULAR INC.

Primary DI Number: 00884999036130
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 878263359 *Terms of Use

Device Description: Abbott RealTime HCV Genotype II Amplification Reagent Kit

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:	Yes
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?
59866	Hepatitis C virus genotyping IVD, kit, nucleic acid technique (NAT)	A collection of reagents and other associated materials intended to be used for the genotype determination of Hepatitis C virus in a clinical specimen, using a nucleic acid technique (NAT).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OBF	Assay, genotyping, hepatitis c virus

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P120012	001
P120012	002
P120012	003
P120012	004
P120012	005
P120012	006
P120012	007
P120012	009
P120012	010
P120012	011
P120012	012
P120012	013
P120012	014
P120012	015
P120012	016
P120012	017
P120012	018

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 -25 and -15 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e616a641-ceff-4728-82aa-01bf86af6e2c
Public Version Date: November 08, 2019
Public Version Number: 4
DI Record Publish Date: November 20, 2014

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

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

[?]

Phone: +1(800)553-7042
Email: customerservice@abbottmolecular.com

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