Primary Device ID | 20681490138639 |
NIH Device Record Key | abcb7d48-a17d-4184-8617-f56561778ce9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BRIDGEMASTER® |
Version Model Number | 600306 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490138635 [Primary] |
GS1 | 20681490138639 [Package] Contains: 00681490138635 Package: PK [5 Units] In Commercial Distribution |
EPP | SPLINT, NASAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2017-09-09 |
20681490138639 | SPLINT 600306 BRIDGEMASTER 5PK LARGE |
20681490138622 | SPLINT 600302 BRIDGEMASTER 5PK SMALL |