Primary Device ID | 00850024135055 |
NIH Device Record Key | a77361bd-74c1-4178-a087-a32050d521d1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Strauss Sugical |
Version Model Number | STS-LAP-202-54 |
Company DUNS | 024725124 |
Company Name | AMERICAN MEDICAL ENDOSCOPY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00850024135055 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00850024135055]
Moist Heat or Steam Sterilization
[00850024135055]
Moist Heat or Steam Sterilization
[00850024135055]
Moist Heat or Steam Sterilization
[00850024135055]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-10 |
Device Publish Date | 2020-11-02 |
00810143892512 - Strauss Surgical | 2024-04-16 |
00810143892529 - Strauss Surgical | 2024-04-16 |
00810143891584 - Strauss Surgical | 2023-12-13 |
00810143891591 - Strauss Surgical | 2023-12-13 |
00810143891607 - Strauss Surgical | 2023-12-13 |
00810143891614 - Strauss Surgical | 2023-12-13 |
00810143891621 - Strauss Surgical | 2023-12-13 |
00810143891638 - Strauss Surgical | 2023-12-13 |