FULL ECHO® PRO 1326801
GUDID 03700111425422
03 pieces sets for embryo transfer
LABORATOIRE CCD
Assisted reproduction transfer catheter trial| Primary Device ID | 03700111425422 |
| NIH Device Record Key | 44e5d77f-fa3a-47e6-9c1e-2c1e63d5cc94 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FULL ECHO® PRO |
| Version Model Number | FULL ECHO® PRO |
| Catalog Number | 1326801 |
| Company DUNS | 381633924 |
| Company Name | LABORATOIRE CCD |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com | |
| Phone | +33(0)344266369 |
| Infomed@ccdlab.com |
Device Dimensions
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
| Catheter Length | 27.4 Centimeter |
| Outer Diameter | 0.155 Centimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *-The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place. |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700111400429 [Primary] |
| GS1 | 03700111425422 [Package] Contains: 03700111400429 Package: Box [10 Units] In Commercial Distribution |
FDA Product Code
| MQF | CATHETER, ASSISTED REPRODUCTION |
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 | 2023-12-13 |
| Device Publish Date | 2023-12-05 |
Devices Manufactured by LABORATOIRE CCD
| 03700111401099 - RIGISTER CUPULE 20 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401105 - RIGISTER CUPULE 25 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401112 - RIGISTER CUPULE 30 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401129 - RIGISTER CUPULE 35 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401136 - SLIDING RIGISTER CUPULE 20 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401143 - SLIDING RIGISTER CUPULE 25 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401150 - SLIDING RIGISTER CUPULE 30 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
| 03700111401167 - SLIDING RIGISTER CUPULE 35 mm | 2025-12-05 Device for hysterosalpingography and chromopertubation |
Trademark Results [FULL ECHO]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FULL ECHO 87935239 not registered Live/Pending |
PRODIMED 2018-05-24 |
 FULL ECHO 79089330 4058131 Dead/Cancelled |
PRODIMED 2010-09-24 |
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