Integra
GUDID B504GS1002510
Provision
Drilling power tool attachment, basic| Primary Device ID | B504GS1002510 |
| NIH Device Record Key | e5370f1e-a492-4adb-ad0f-160dae6efbf5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integra |
| Version Model Number | 100-251 |
| 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 | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com | |
| Phone | 541-508-7520 |
| customersupport@provisiondrs.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504GS1002510 [Primary] |
FDA Product Code
| KDC | Instrument, Surgical, Disposable |
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 [Integra]
| B504CT0800030 | 08-0003 |
| B5040800030 | 08-0003 |
| 08100410609113 | 08-0003 |
| 00810041069108 | 08-0003 |
| B504OM6007090 | 60-0709 |
| B504OMSAW6949T0 | SAW6949T |
| B504OMSAW6948T0 | SAW6948T |
| B504OMSAW6945T0 | SAW6945T |
| B504OMLJV528T0 | LJV528T |
| B504OMLJV527T0 | LJV527T |
| B504OMLJV526T0 | LJV526T |
| B504OMLJV525T0 | LJV525T |
| B504OMSAW6951T0 | SAW6951T |
| B504OM2502620 | 250-262 |
| B504OM2502610 | 250-261 |
| B504OMPAN101000340 | PAN-1010-0034 |
| B504OM35392520 | 3539252 |
| B504OM33340 | 33-34 |
| B504OMLJU097T0 | LJU097T |
| B504OMSAW6947T0 | SAW6947T |
| B504OM25026500 | 250-2650 |
| B504GS4601070 | 460-107 |
| B504GS1101800 | 110-180 |
| B504GS1005430 | 100-543 |
| B504GS1991050 | 199-105 |
| B504GS37244030 | 3724403 |
| B504GS1091190 | 109-119 |
| B504GS1072200 | 107-220 |
| B504GS2041500 | 204-150 |
| B504GS1061310 | 106-131 |
| B504OM1302340 | 130-234 |
| B504GSMH61200 | MH6-120 |
| B504GS2504100 | 250-410 |
| B504GS2503980 | 250-398 |
| B504GS1013000 | 101-300 |
| B504CT0961000 | 09-6100 |
| B504GS2853800 | 285-380 |
| B504GS1101180 | 110-118 |
| B504GS1032200 | 103-220 |
| B504GS2854520 | 285-452 |
| B504OM4103020 | 410-302 |
| B504OM4103010 | 410-301 |
| B504GS1061300 | 106-130 |
| B504GS1002510 | 100-251 |
| B504GS1002120 | 100-212 |
| B504GS4801050 | 480-105 |
Trademark Results [Integra]
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