ConMed
GUDID B504SRSMI02N0
Provision
Suturing unit, reprocessed| Primary Device ID | B504SRSMI02N0 |
| NIH Device Record Key | 0ca3de4a-c7cb-4e8e-8a41-e5ddb614b953 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ConMed |
| Version Model Number | SMI-02N |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504SRSMI02N0 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-11-25 |
| Device Publish Date | 2021-11-17 |
On-Brand Devices [ConMed]
Trademark Results [ConMed]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONMED 87743956 not registered Live/Pending |
ConMed Corporation 2018-01-04 |
 CONMED 87551457 5467478 Live/Registered |
ConMed Corporation 2017-08-01 |
 CONMED 87013011 5304308 Live/Registered |
ConMed Corporation 2016-04-25 |
 CONMED 75292291 2213939 Live/Registered |
ConMed Corporation 1997-05-15 |
 CONMED 73000298 1004240 Live/Registered |
CONSOLIDATED MEDICAL EQUIPMENT, INC. 1973-09-06 |
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