KMEDIC KM54313
GUDID 24026704285628
MEYHOEFFER CURETTE 5" #2 2.0 MILLIMETER
TELEFLEX INCORPORATED
Ophthalmic curette, reusable| Primary Device ID | 24026704285628 |
| NIH Device Record Key | 7a5e2044-fffb-4090-b144-32fb9515a5a1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KMEDIC |
| Version Model Number | IPN015124 |
| Catalog Number | KM54313 |
| Company DUNS | 002348191 |
| Company Name | TELEFLEX INCORPORATED |
| 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(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
| Length | 12.7 Centimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04026704285624 [Direct Marking] |
| GS1 | 24026704285628 [Primary] |
FDA Product Code
| HNZ | Curette, ophthalmic |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
[24026704285628]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-06-07 |
| Device Publish Date | 2018-09-15 |
On-Brand Devices [KMEDIC]
| 24026704607161 | COMFORT RATCHETING T-HANDLE SCREWDRIVER |
| 24026704607154 | MULTI-PURPOSE T-HANDLE |
| 24026704607147 | HEX DRIVER FEMALE - 15.0 MILLIMETER |
| 24026704607130 | HEX DRIVER FEMALE - 13.0 MILLIMETER |
| 24026704607123 | HEX DRIVER FEMALE 7.5 MILLIMETER |
| 24026704607116 | ISOLA-CLOSED DRIVER |
| 24026704607109 | ISOLA-OPEN DRIVER |
| 24026704607093 | MONARCH PEDICLE DRIVER |
| 24026704607086 | X25 HEXALOBE DRIVER |
| 24026704607079 | X20 HEXALOBE DRIVER |
| 24026704607062 | BROKEN SCREW REMOVER FOR 8 MILLIMETER SCREW |
| 24026704607055 | BROKEN SCREW REMOVER FOR 7 MILLIMETER SCREW |
| 24026704607048 | BROKEN SCREW REMOVER FOR 6 MILLIMETER SCREW |
| 24026704607031 | BROKEN SCREW REMOVER FOR 5 MILLIMETER SCREW |
| 24026704607024 | BROKEN SCREW REMOVER FOR 4 MILLIMETER SCREW |
| 24026704607017 | TREPHINES FOR 8 MILLIMETER SCREW |
| 24026704607000 | TREPHINES FOR 7 MILLIMETER SCREW |
| 24026704606997 | TREPHINES FOR 6 MILLIMETER SCREW |
| 24026704606980 | TREPHINES FOR 5 MILLIMETER SCREW |
| 24026704606973 | TREPHINES FOR 4 MILLIMETER SCREW |
| 24026704606966 | SCREW EXTRACTOR 3.5 MILLIMETER HEX |
| 24026704606959 | SCREW EXTRACTOR 3.0 MILLIMETER HEX |
| 24026704606942 | SCREW EXTRACTOR 2.5 MILLIMETER HEX |
| 24026704606935 | MEDIUM BLADE DRIVER |
| 24026704606928 | HEXALOBE DRIVER T40 |
| 24026704606911 | HEXALOBE DRIVER T30 |
| 24026704606904 | HEXALOBE DRIVER T25 |
| 24026704606898 | HEXALOBE DRIVER T20 |
| 24026704606881 | HEX DRIVER- FEMALE 1/2" (12.70 MILLIMETER) |
| 24026704606874 | HEX DRIVER- FEMALE 7/16" (11.11 MILLIMETER) |
| 24026704606867 | HEX DRIVER- FEMALE 3/8" (9.53 MILLIMETER) |
| 24026704606850 | HEX DRIVER- FEMALE 5/16" (7.94 MILLIMETER) |
| 24026704606843 | HEX DRIVER- FEMALE 1/4" (6.35 MILLIMETER) |
| 24026704606836 | HEX DRIVER- FEMALE 7/32" (5.56 MILLIMETER) |
| 24026704606829 | HEX DRIVER- FEMALE 3/16" (4.76 MILLIMETER) |
| 24026704606812 | HEX DRIVER- FEMALE 5/32" (3.97 MILLIMETER) |
| 24026704606805 | HEX DRIVER- FEMALE 1/8" (3.18 MILLIMETER) |
| 24026704606799 | HEX DRIVER- FEMALE 10.0 MILLIMETER |
| 24026704606782 | HEX DRIVER- FEMALE 9.0 MILLIMETER |
| 24026704606775 | HEX DRIVER- FEMALE 8.0 MILLIMETER |
| 24026704606768 | HEX DRIVER- FEMALE 7.0 MILLIMETER |
| 24026704606751 | HEX DRIVER- FEMALE 6.0 MILLIMETER |
| 24026704606744 | HEX DRIVER- FEMALE 5.0 MILLIMETER |
| 24026704606737 | HEX DRIVER- MALE 1/4" (6.35 MILLIMETER) |
| 24026704606720 | HEX DRIVER- MALE 7/32" (5.56 MILLIMETER) |
| 24026704606713 | HEX DRIVER- MALE 3/16" (4.76 MILLIMETER) |
| 24026704606706 | HEX DRIVER-MALE 5/32" (3.97 MILLIMETER) |
| 24026704606690 | HEX DRIVER- MALE 1/8" (3.18 MILLIMETER) |
| 24026704606683 | HEX DRIVER- MALE 7/64" (2.78 MILLIMETER) |
| 24026704606676 | HEX DRIVER-MALE 7.0 MILLIMETER |
Trademark Results [KMEDIC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KMEDIC 74637968 1965338 Dead/Cancelled |
K-Medic, Inc. 1995-02-22 |
 KMEDIC 74637955 1966576 Live/Registered |
TELEFLEX INCORPORATED 1995-02-22 |
 KMEDIC 74533291 1940595 Live/Registered |
TELEFLEX INCORPORATED 1994-06-06 |
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