Primary Device ID | B504OMS8976750 |
NIH Device Record Key | b418c66e-6a07-4978-8e53-f87604bdaf8b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | De Soutter |
Version Model Number | S89-7675 |
Company DUNS | 016889401 |
Company Name | Provision |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B504OMS8976750 [Primary] |
GFA | Blade, Saw, General & Plastic Surgery, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-23 |
Device Publish Date | 2020-09-15 |
B504OMS8976750 | S89-7675 |
B504OMS8966360 | S89-6636 |
B504OMS8605150 | S86-0515 |
B504OMS843600 | S84-360 |
00810041638632 | S89-7675 |
00810041638625 | S89-6636 |
00810041638618 | S86-0515 |
00810041638601 | S84-360 |
B504OMS8915730 | S89-1573 |
00810041639776 | S89-1573 |