Primary Device ID | 07332747208566 |
NIH Device Record Key | f0a69500-f678-4b33-be1c-83425c2d8870 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Unigrip™ |
Version Model Number | 29150 |
Catalog Number | 29150 |
Company DUNS | 353939929 |
Company Name | Nobel Biocare AB |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com | |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Length | 36 Millimeter |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07332747208566 [Primary] |
NDP | Accessories, implant, dental, endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
[07332747208566]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-31 |
Device Publish Date | 2025-07-23 |
07332747009088 | Screwdriver Manual UniGrip 36 mm |
07332747009071 | Screwdriver Manual UniGrip 28 mm |
07332747009064 | Screwdriver Manual UniGrip 20 mm |
07332747029833 | Screwdriver Machine UniGrip 20 mm |
07332747009002 | Screwdriver Machine UniGrip 35 mm |
07332747008999 | Screwdriver Machine UniGrip 30 mm |
07332747008982 | Screwdriver Machine UniGrip 25 mm |
07332747208603 | Screwdriver Machine UniGrip™ 35 mm |
07332747208597 | Screwdriver Machine UniGrip™ 30 mm |
07332747208580 | Screwdriver Machine UniGrip™ 25 mm |
07332747208573 | Screwdriver Machine UniGrip™ 20 mm |
07332747208566 | Screwdriver Manual UniGrip™ 36 mm |
07332747208559 | Screwdriver Manual UniGrip™ 28 mm |
07332747208542 | Screwdriver Manual UniGrip™ 20 mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() UNIGRIP 98890329 not registered Live/Pending |
QINGDAO GRIP TYRE CO., LTD. 2024-12-07 |
![]() UNIGRIP 87776409 not registered Live/Pending |
Lawson Products, Inc. 2018-01-30 |
![]() UNIGRIP 86233854 4771314 Live/Registered |
Robert Craig Hawkins 2014-03-27 |
![]() UNIGRIP 85725428 not registered Dead/Abandoned |
QINGDAO GRIP TYRE CO,. LTD. 2012-09-11 |
![]() UNIGRIP 78225698 not registered Dead/Abandoned |
C. R. Bard, Inc. 2003-03-14 |
![]() UNIGRIP 78094522 2756071 Dead/Cancelled |
James & Alden Plc 2001-11-21 |
![]() UNIGRIP 77848233 not registered Dead/Abandoned |
Linx Ltd 2009-10-14 |
![]() UNIGRIP 74325151 1775321 Dead/Cancelled |
MINIGRIP, INC. 1992-10-19 |
![]() UNIGRIP 74320448 1845094 Dead/Cancelled |
UNISURGE, INC. 1992-10-07 |
![]() UNIGRIP 73543855 1376037 Dead/Cancelled |
MINIGRIP, INC. 1985-06-19 |
![]() UNIGRIP 72336613 0952542 Live/Registered |
ARTHUR G. RUSSELL COMPANY, INCORPORATED, THE 1969-08-28 |