| Primary Device ID | 00192896122574 |
| NIH Device Record Key | 64ea5b56-b26f-48fe-84e6-f4b632f014b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Maryland Grasping Forceps |
| Version Model Number | 2901-213L |
| Catalog Number | 2901-213L |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)821-7496 |
| info@sontecinstruments.com |
| Outer Diameter | 5 Millimeter |
| Length | 450 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896122574 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896122574]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-01-30 |
| Device Publish Date | 2026-01-22 |
| B0992901202S0 | MARYLAND GRASPING FORCEPS DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| B0992901202L0 | MARYLAND GRASPING FORCEPS DOUBLE-ACTION JAWS FOR TUBE SHAFT |
| 00192896115040 | Maryland Grasping Forceps Double Action Jaw Insert For 10 Millimeter Diameter Tube Shaft |
| 00192896122574 | Maryland Grasping Forceps Double Action Jaws 17.5 Millimeter Jaw Length |