| Primary Device ID | 00887482139110 |
| NIH Device Record Key | ccea857c-f2c4-4ae7-aa17-0d944dad33b3 |
| Commercial Distribution Discontinuation | 9999-01-01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symmetry Gerald |
| Version Model Number | 08-0013I |
| Catalog Number | 08-0013I |
| Company DUNS | 079641356 |
| Company Name | SYMMETRY SURGICAL INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| 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 | true |
| 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 | 00887482139110 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887482139110]
Moist Heat or Steam Sterilization
[00887482139110]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-05-24 |
| 00887482139509 | Bayonet Bipolar Forceps 7 1/2" (190.5Mm) Irrigating And Insulated With A (High Polished 10Mm Lon |
| 00887482139493 | Bayonet Bipolar 1.0 mm Tip 7 1/2 Inches Irrigated |
| 00887482139127 | Bayonet Bipolar Forceps 1.0 mm 7 1/2 Inches Insulated, Irrigated |
| 00887482139110 | Bayonet Bipolar Forceps 1.0 mm 7.25 Inches Insulated |
| 00887482035931 | BAYONET BIPOLAR FORCEP 1.0MM 7 1/2" |
| 00887482035924 | Bipolar Forceps Straight 1.0 Mm 7 Inches |