AccessGUDID - DEVICE: multiSTATION™ (00850012846413)

GUDID

Device Identifier (DI) Information

Brand Name: multiSTATION™
Version or Model: 081890
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 081890
Company Name: LSI Solutions, Inc.

Primary DI Number: 00850012846413
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 603420183 *Terms of Use

Device Description: 5MM Cannula with Obturator

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:	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?
62857	Pleuroscopic/mediastinoscopic access cannula, reusable	A rigid, single-lumen, surgical instrument intended to be percutaneously inserted through the chest to provide access to the pleural and/or mediastinal cavity to facilitate the introduction of surgical instruments as part of a minimally-invasive procedure; it is not intended for pericardial access. It provides an entry between adjacent ribs and once in place is intended to remain in position for the duration of the procedure. It may include a trocar with a sharp or blunt tip intended to assist introduction; devices with the trocar included it may be referred to as a trocar or trocar assembly. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MDM	INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: ceb589ac-e847-43df-aec4-35cef3b111b6
Public Version Date: February 07, 2025
Public Version Number: 1
DI Record Publish Date: January 30, 2025

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: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(866)575-3493
Email: regulatorydpt@lsisolutions.com

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