Primary Device ID | 00889024016071 |
NIH Device Record Key | 06d7d7b1-fd15-46d2-833a-450f35e47037 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SwissPlus® |
Version Model Number | OPWSCL |
Company DUNS | 103167086 |
Company Name | ZIMMER DENTAL INC. |
Device Count | 1 |
DM Exempt | true |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024016071 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-10-09 |
00889024017559 | SPSCS |
00889024017542 | SPSCL |
00889024017535 | SPSC |
00889024017443 | SPMA2 |
00889024017412 | SPGA |
00889024016071 | OPWSCL |
00889024016064 | OPWSC |
00889024015999 | OPSCS |
00889024015982 | OPSCL |
00889024015975 | OPSC |
00889024015944 | OPH20S |
00889024015937 | OPH20 |
00889024015920 | OPGC |
00889024015913 | OPGA |
00889024015845 | OPBA3 |
00889024015838 | OPBA |
00889024015784 | OPAS |
00889024015760 | OPACT3 |
00889024015753 | OPACT |
00889024015722 | OPA2 |
00889024015715 | OPA |
00889024014947 | GPCAS |
00889024020320 | WSX |
00889024017528 | SPMT |
00889024017450 | SPMAR |
00889024016095 | OTL3.0-S |
00889024016088 | OT3.0-S |
00889024016057 | OPWB8 |
00889024016040 | OPWB14 |
00889024016033 | OPWB12 |
00889024016026 | OPWB10 |
00889024016019 | OPT/5 |
00889024015968 | OPS |
00889024015883 | OPCC |
00889024015876 | OPC |
00889024015869 | OPBAT |
00889024015821 | OPB8 |
00889024015814 | OPB14 |
00889024015807 | OPB12 |
00889024015791 | OPB10 |
00889024015746 | OPA/6 |
00889024015739 | OPA/5 |
00889024015272 | HLRTX2 |
00889024014923 | FMTM2 |
00889024014886 | FMSW |
00889024014879 | FMSM |
00889024014862 | FMS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SWISSPLUS 75908000 2791712 Live/Registered |
ZIMMER DENTAL INC. 2000-02-01 |