Primary Device ID | 04560264516502 |
NIH Device Record Key | 9a9f2509-0c23-497e-8543-d59ea95dfaeb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NSK Sterile Blades |
Version Model Number | PDS-RE-4223 |
Company DUNS | 690710546 |
Company Name | NAKANISHI 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *Store in a place avoiding direct sunlight and high temperatures humidity without any extreme loads. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04560264516502 [Primary] |
HBC | MOTOR, DRILL, ELECTRIC |
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 |
04560264548534 | PDS-RE-4028E |
04560264548527 | PDS-RE-4023E |
04560264516625 | PDS-SO-653 |
04560264516502 | PDS-RE-4223 |
04560264516496 | PDS-RE-4217 |
04560264516489 | PDS-RE-4114 |
04560264516472 | PDS-RE-4028 |
04560264516465 | PDS-RE-4023 |
04560264516458 | PDS-RE-6127 |
04560264516441 | PDS-RE-4127 |
04560264516434 | PDS-OSC-432 |
04560264516427 | PDS-OSC-422 |
04560264516410 | PDS-SO-642 |
04560264516403 | PDS-SO-632 |
04560264516380 | PDS-SO-453 |
04560264516373 | PDS-SO-452 |
04560264516366 | PDS-SO-442 |
04560264516359 | PDS-SO-441 |
04560264516342 | PDS-SO-433 |
04560264516335 | PDS-SO-432 |
04560264516328 | PDS-SO-431 |
04560264516311 | PDS-SO-422 |
04560264516304 | PDS-SO-412 |
04560264516298 | PDS-SO-411 |