AccessGUDID - DEVICE: NA (00848838091834)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: 7116-70
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: REMEL, INC.

Primary DI Number: 00848838091834
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 065769564 *Terms of Use

Device Description: MYCO PZA 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):	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?
62407	Anti-tuberculosis (anti-TB) drug susceptibility testing reagent kit IVD	A collection of reagents and other associated materials intended to be added to a culture medium containing a culture isolate of Mycobacteruim tuberculosis from a clinical specimen, to determine antimicrobial susceptibility to an anti-tuberculosis drug [e.g., pyrazinamide (PZA)].	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MJA	Susceptibility Test Powders, Antimycobacterial

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K052323	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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: d2982896-85ce-4b54-85fd-57745063a235
Public Version Date: November 15, 2021
Public Version Number: 4
DI Record Publish Date: December 09, 2016

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: 8002556730
Email: csemail@thermofisher.com

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