UNBRANDED
GUDID 10848340009690
Snap Kap
ADVANCE MEDICAL DESIGNS, INC.
Instrument/equipment drape, single-use, sterile| Primary Device ID | 10848340009690 |
| NIH Device Record Key | 3a784c88-a760-455a-ba42-3141516babe7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNBRANDED |
| Version Model Number | KP09LNS |
| Company DUNS | 130785884 |
| Company Name | ADVANCE MEDICAL DESIGNS, INC. |
| Device Count | 1 |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00848340009693 [Primary] |
| GS1 | 10848340009690 [Package] Contains: 00848340009693 Package: [200 Units] In Commercial Distribution |
FDA Product Code
| JAA | System, x-ray, fluoroscopic, image-intensified |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10848340009690]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-28 |
On-Brand Devices [UNBRANDED]
Trademark Results [UNBRANDED]
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