Primary Device ID | D909700001T1 |
NIH Device Record Key | 804b2cab-eab5-4962-ae9b-a09411632121 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WIRE BONDER |
Version Model Number | 700-001T |
Catalog Number | 700-001T |
Company DUNS | 020956330 |
Company Name | Ortho Arch Company Inc |
Device Count | 1 |
DM Exempt | false |
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 | false |
Expiration Date | false |
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 | D909700001T1 [Primary] |
EGD | Wax, Dental, Intraoral |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-05 |
Device Publish Date | 2023-06-27 |
D909700001T1 | WIRE BONDER LG TIP |
D9097000011 | WIRE BONDER LG TIPS & HANDLE (10 TIPS) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WIRE BONDER 75015037 not registered Dead/Abandoned |
WOLK, ROGER 1995-11-06 |