AccessGUDID - DEVICE: Data Logger Bravo (G) (07540196002387)

GUDID

Device Identifier (DI) Information

Brand Name: Data Logger Bravo (G)
Version or Model: 01-111729
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 01-111729
Company Name: Scican Ltd

Primary DI Number: 07540196002387
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 204137145 *Terms of Use

Device Description: Data logger for Bravo Chamber Autoclave

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?
46563	Digital storage media	A portable electronic device designed to record and store data from an electronic source (e.g., a computer), storing the information in a digital format so that the data can be copied or retrieved (read or downloaded) using computer technology. It may be one of a variety of formats (e.g., recordable DVD, recordable CD, USB flash drive, MO disc, UDO disc, floppy disc).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OUG	Medical Device Data System

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: 230f1d72-4938-42a6-88a7-36273fe781b2
Public Version Date: February 23, 2022
Public Version Number: 1
DI Record Publish Date: February 15, 2022

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

Customer Contact

[?]

Phone: 18006677733
Email: tboyce@scican.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES