AccessGUDID - DEVICE: ALAR® (00763000038182)

GUDID

Device Identifier (DI) Information

Brand Name: ALAR®
Version or Model: 15000
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MEDTRONIC XOMED, INC.

Primary DI Number: 00763000038182
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 835465063 *Terms of Use

Device Description: STENT 15000 2PK ALAR NASALVALVE COLLAPSE

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:	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?
62718	Intranasal splinting set	A collection of sterile, non-biodegradable devices intended to temporarily support and immobilize intranasal tissues during the postoperative healing period following intranasal and nasal valve surgery. It consists of a synthetic polymer splint designed to be surgically placed into the nasal cavity, via a nostril, with included suture and needle. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LYA	SPLINT, INTRANASAL SEPTAL

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K151758	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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
Height: 0.5 Millimeter
Width: 16.0 Millimeter
Length: 19.0 Millimeter

Device Record Status

Public Device Record Key: c508b80a-48d7-46fa-b5ea-fc8cbea98e36
Public Version Date: October 23, 2020
Public Version Number: 1
DI Record Publish Date: October 15, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20763000038186	2	00763000038182		In Commercial Distribution	PK

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: +1(800)633-8766
Email: Corporate.UDI@medtronic.com

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

FDA TOOLS & RESOURCES