| Primary Device ID | 35713311000121 |
| NIH Device Record Key | adf8dfa1-14c0-4f98-bc9a-20e323ed6d5b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NUNC IVF MULTIDISH 4 WELL NUNCLON |
| Version Model Number | 144444 |
| Company DUNS | 305971764 |
| Company Name | Nunc A/S |
| Device Count | 4 |
| DM Exempt | false |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15713311000127 [Primary] |
| GS1 | 35713311000121 [Package] Contains: 15713311000127 Package: Case [30 Units] In Commercial Distribution |
| GS1 | 85713311000126 [Unit of Use] |
| MQK | LABWARE, ASSISTED REPRODUCTION |
| PUD | Labware, Assisted Reproduction, Exempt |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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[35713311000121]
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| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-22 |
| Device Publish Date | 2018-09-21 |
| 05713311000014 | The Nunc IVF Multidish 4-Well Nunclon is a injection moulded polystyrene plate. The material is |
| 35713311000121 | NUNC IVF MULTIDISH 4 WELL NUNCLON |