CrossRoads
GUDID B504OM1305040
Provision
Burring power tool attachment| Primary Device ID | B504OM1305040 |
| NIH Device Record Key | cf0a9194-59b7-40d6-9242-24f6dc873eef |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CrossRoads |
| Version Model Number | 130504 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OM1305040 [Primary] |
FDA Product Code
| HTO | Reamer |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-03 |
| Device Publish Date | 2024-08-26 |
On-Brand Devices [CrossRoads]
| B504OM710025000 | 7100-2500 |
| B504OM710020000 | 7100-2000 |
| B504OM710018000 | 7100-1800 |
| B504OM710015000 | 7100-1500 |
| B504OM700040SB0 | 7000-40SB |
| B504OM2460020 | 246002 |
| B504OM2470020 | 247002 |
| B504OM2451100 | 245110 |
| B504OM2451070 | 245107 |
| B504OM2451060 | 245106 |
| B504OM2450660 | 245066 |
| B504OM2450650 | 245065 |
| B504OM2450560 | 245056 |
| B504OM2450550 | 245055 |
| B504OM1305170 | 130517 |
| B504OM1305050 | 130505 |
| B504OM1305040 | 130504 |
| B504OM1305030 | 130503 |
| B504OM1212250 | 121225 |
| B504OM150047010 | 1500-4701 |
| B504OM1305280 | 130528 |
| B504OM1305000 | 130500 |
Trademark Results [CrossRoads]
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