Diacap® 720DH13G
GUDID 04046955659616
Diacap Pro 13H
B.Braun Avitum AG
Hollow-fibre haemodialysis dialyser, single-use| Primary Device ID | 04046955659616 |
| NIH Device Record Key | 11fa0211-959c-4d38-bc61-d2800d8aa5bb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Diacap® |
| Version Model Number | 720DH13G |
| Catalog Number | 720DH13G |
| Company DUNS | 343689704 |
| Company Name | B.Braun Avitum AG |
| Device Count | 20 |
| DM Exempt | true |
| Pre-market Exempt | false |
| 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 | false |
| 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 | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com | |
| Phone | +1(800)848-2066 |
| rtd.us@bbraun.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046955659616 [Unit of Use] |
| GS1 | 04046955659623 [Primary] |
FDA Product Code
| KDI | Dialyzer, high permeability with or without sealed dialysate system |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-07-26 |
| Device Publish Date | 2022-09-16 |
On-Brand Devices [Diacap®]
| 04046964610837 | Diacap® Pro 16H |
| 04046964610813 | Diacap® Pro 19H |
| 04046964610776 | Diacap® Pro 13H |
| 04046964319983 | DIACAP HIPS 12 PS DIALYZER |
| 04046964319921 | Diacap? Polysulfone® LOPS 12 |
| 04046964319891 | DIACAP LOPS 10 PS DIALYZER |
| 04046964320002 | Diacap Polysulfone® HI PS 15 Dialyzer |
| 04046964319969 | Diacap Polysulfone® HI PS 10 Dialyzer |
| 04046964319945 | Diacap Polysulfone® LO PS 15 Dialyzer |
| 04039239090496 | Diacap® Ultra Dialysis Fluid Filters |
| 04046964320040 | Diacap Polysulfone® HI PS 20 Dialyzer |
| 04046964320026 | Diacap Polysulfone® HI PS 18 Dialyzer |
| 04046963178109 | DIACAP ULTRA DF FILTER CA & US |
| 04046955659654 | Diacap Pro 19H |
| 04046955659630 | Diacap Pro 16H |
| 04046955659616 | Diacap Pro 13H |
Trademark Results [Diacap]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DIACAP 79031949 3366116 Live/Registered |
B. Braun Avitum AG 2006-11-07 |
 DIACAP 74573962 not registered Dead/Abandoned |
Ciba-Geigy Corporation 1994-09-15 |
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