POPLOK BKL-00M
GUDID 20845854030353
2.8MM POPLOK DRILL BIT
Conmed Corporation
Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable| Primary Device ID | 20845854030353 |
| NIH Device Record Key | d54a84a9-6712-405c-8b01-f5a17f820f96 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | POPLOK |
| Version Model Number | BKL-00M |
| Catalog Number | BKL-00M |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 |
Customer Support Contacts
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
Device Dimensions
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
| Outer Diameter | 2.8 Millimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854030356 [Primary] |
| GS1 | 20845854030353 [Direct Marking] |
FDA Product Code
| GFG | BIT, SURGICAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
[20845854030353]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-02 |
| Device Publish Date | 2020-09-24 |
On-Brand Devices [POPLOK]
| 20845854014285 | 3.3MM SRS POPLOK, SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE |
| 20845854014124 | 4.5MM POPLOK SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES |
| 20845854014117 | 2.8MM SRS POPLOK SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE |
| 20845854014100 | 4.5MM POPLOK SUTURE ANCHOR |
| 20845854013998 | 3.3MM SRS POPLOK, SUTURE ANCHOR WITH TWO NO. 0 (3.5 METRIC) HI-FI SUTURES |
| 20845854013851 | 3.5MM SRS POPLOK SUTURE ANCHOR |
| 20845854013714 | 3.5MM POPLOK SUTURE ANCHOR WITH ONE NO. 2, (5 METRIC) HI-FI SUTURE |
| 20845854013554 | 2.8MM SRS POPLOK, SUTURE ANCHOR WITH TWO NO. 0 (3.5 METRIC) HI-FI SUTURES |
| 20845854030353 | 2.8MM POPLOK DRILL BIT |
| 20845854030346 | POPLOK DRILL GUIDE |
| 20845854028282 | POPLOK PUNCH 4.5MM |
| 20845854028275 | POPLOK PUNCH 3.5MM |
| 10845854030370 | POPLOK OBTURATOR |
| 10845854028292 | PopLok Punch with Depth Stop |
Trademark Results [POPLOK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 POPLOK 77740905 3770304 Live/Registered |
PAX IP INC. 2009-05-20 |
 POPLOK 77717288 3880771 Live/Registered |
CONMED CORPORATION 2009-04-20 |
 POPLOK 74579586 1954480 Dead/Cancelled |
Gianni Enterprises, Inc. 1994-09-28 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.