| Primary Device ID | B0992901202L0 |
| NIH Device Record Key | 95c73249-6755-4123-bdc4-1efacced7b5e |
| Commercial Distribution Discontinuation | 2018-06-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MARYLAND GRASPING FORCEPS |
| Version Model Number | 2901-202L |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 800-821-7496 |
| info@sontecinstruments.com | |
| Phone | 800-821-7496 |
| info@sontecinstruments.com |
| Length | 330 Millimeter |
| Device Size Text, specify | 0 |
| Length | 330 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B0992901202L0 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B0992901202L0]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0992901202L0]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 7 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-19 |
| 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 |