AccessGUDID - DEVICE: TIO™ (10884450122782)

GUDID

Device Identifier (DI) Information

Brand Name: TIO™
Version or Model: 10884450122782
Commercial Distribution Status: In Commercial Distribution
Catalog Number: TIO60-110
Company Name: Merit Medical Systems, Inc.

Primary DI Number: 10884450122782
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 10
Labeler D-U-N-S® Number*: 184763290 *Terms of Use

Device Description: No description.

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?
47162	Endoscopic bite block, oxygenating	A dual-purpose device inserted into a patient's mouth to maintain oral patency during an endoscopic procedure primarily to protect the endoscope, introduced via the mouth, from the patient's natural tendency to bite down on the instrument, and that simultaneously supports an oxygen (O2) line to provide the patient with an uninterrupted flow of O2 during and after endoscopy. The device also protects the tongue and teeth of the patient during endoscopy and may include a gas sample line that enables monitoring of the expired carbon dioxide (CO2) during the procedure. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MNK	Endoscopic bite block

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
Device Size Text, specify: Blade Length-110 mm

Device Record Status

Public Device Record Key: 108fcad1-a8d8-41ba-a8f3-f0fd611b2a8c
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: February 16, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20884450122789	4	10884450122782		In Commercial Distribution

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: 00884450122785 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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