Primary Device ID | 00857910006581 |
NIH Device Record Key | 69a422d2-0d2f-4643-b07c-bab59a792c1a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ALP® |
Version Model Number | ALP® 1P |
Catalog Number | 500019 |
Company DUNS | 079598595 |
Company Name | CURRIE MEDICAL SPECIALTIES INC. |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857910006086 [Primary] |
GS1 | 00857910006581 [Package] Contains: 00857910006086 Package: Case 10 Pr [20 Units] In Commercial Distribution |
JOW | Sleeve, Limb, Compressible |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-05 |
Device Publish Date | 2019-07-26 |
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