Primary Device ID | 00841912100163 |
NIH Device Record Key | 0928d2ce-5316-42b3-b68c-1fb1646f9eec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PullUp Probe Cover Kit |
Version Model Number | 2097 |
Catalog Number | 2097 |
Company DUNS | 965417181 |
Company Name | PROTEK MEDICAL PRODUCTS, 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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00841912100163 [Primary] |
GS1 | 10841912100160 [Package] Package: [24 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
10841912105653 | 2211 |
10841912105363 | 2295 |
00841912104475 | 2097 |
10841912104359 | 1512 |
10841912102867 | 2231 |
10841912102874 | 2231 |
10841912100627 | 1096 |
10841912100382 | 2233 |
10841912100375 | 2233 |
10841912100368 | 2231 |
10841912100207 | 2099 |
00841912100194 | 2099 |
00841912100187 | 2097 |
10841912100177 | 2097 |
00841912100163 | 2097 |
10841912100153 | 2096 |
00841912100149 | 2095 |
10841912106735 | 2048 |
10841912106315 | 2044 |