Primary Device ID | 10841912100573 |
NIH Device Record Key | 989d6790-9466-4198-b68c-db8dcdbe0acd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Probe Cover Kit |
Version Model Number | 1026 |
Catalog Number | 1026 |
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 | 00841912100576 [Primary] |
GS1 | 10841912100573 [Package] Contains: 00841912100576 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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
10841912105677 | 1467 |
00841912104949 | 2221 |
00841912104574 | 1241 |
10841912104274 | 2320 |
10841912100757 | 1460 |
10841912100740 | 1460 |
10841912100733 | 1460 |
10841912100726 | 1460 |
10841912100719 | 1270 |
10841912100702 | 1240 |
10841912100696 | 1236 |
10841912100573 | 1026 |
10841912100474 | 2450 |
10841912100467 | 2450 |
10841912100450 | 2320 |
10841912100443 | 2320 |
10841912100436 | 2290 |
10841912100429 | 2270 |
10841912100412 | 2252 |
10841912100405 | 2250 |
10841912100399 | 2236 |
10841912100351 | 2230 |
10841912100320 | 2220 |
00841912100316 | 2219 |
00841912100309 | 2216 |
00841912100293 | 2220 |
10841912100252 | 2210 |
10841912100245 | 2208 |