LANDANGER
GUDID 03661219339304
LANDANGER
Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable| Primary Device ID | 03661219339304 |
| NIH Device Record Key | fa57a807-8c21-47f9-bbae-ff33936b12c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LANDANGER |
| Version Model Number | C100582 |
| Company DUNS | 299889175 |
| Company Name | LANDANGER |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03661219339304 [Primary] |
FDA Product Code
| DWS | Instruments, Surgical, Cardiovascular |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
[03661219339304]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-08 |
| Device Publish Date | 2024-04-30 |
On-Brand Devices [LANDANGER]
Trademark Results [LANDANGER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LANDANGER 73652566 1480581 Dead/Expired |
LANDANGER (S.A.) 1987-04-01 |
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