Primary Device ID | 10311960708309 |
NIH Device Record Key | 2165b2a6-8751-4795-bcc9-e4329c15e214 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cramer Blister Foam |
Version Model Number | 030907 |
Company DUNS | 007138183 |
Company Name | CRAMER PRODUCTS, INC. |
Device Count | 25 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |