ROOTT

Primary DI
00810149982040
Brand
ROOTT
Company
TRATE LLC
Model
ITHS
Device description
Implant driver, handpiece, XS, R.
Published
2024-11-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
NDPAccessories, Implant, Dental, Endosseous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NDPAccessories, Implant, Dental, EndosseousDental1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810149980411PrimaryGS10
00810149982040Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810149980411008101499804118101499804110810149980411
00810149982040008101499820408101499820400810149982040

GMDN Terms#

Term, Definition table
TermDefinition
Dental prosthesis removal instrumentA non-electric, hand-held dental instrument intended to be used to remove a permanent or temporary cemented dental prosthesis restoration (e.g., crown, denture, bridge) from a tooth or implant abutment; it is not a thermal detacher. It consists of a metallic instrument with a handle and a pointed, angled distal end used to secure the instrument at the margin of the prosthesis to be removed; it may be designed as a manual, pneumatic or spring-loaded instrument whereby light force is applied to detach the restoration. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Keep away from sunlight
Special Storage Condition, Specify00Keep dry

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
129946338
Device count
5
DM exempt
true
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810149982149ROOTTGF32025-10-23
00810149982170ROOTTD42142025-10-23
00810149982187ROOTTA12025-10-23
00810149982200ROOTTA22025-10-23
00810149982224ROOTTA32025-10-23
00810149982248ROOTTA42025-10-23
00810149982262ROOTTA1A152025-10-23
00810149982286ROOTTA1A252025-10-23
00810149982309ROOTTD20122025-10-23
00810149982323ROOTTD20142025-10-23
00810149982347ROOTTIT2025-10-23
00810149982361ROOTTD25162025-10-23
00810149982385ROOTTD28162025-10-23
00810149982408ROOTTD46162025-10-23
00810149982422ROOTTA2A152025-10-23
00810149982446ROOTTA2A252025-10-23
00810149982460ROOTTTR2025-10-23
00810149982484ROOTTA3A152025-10-23
00810149982507ROOTTA4A152025-10-23
00810149982521ROOTTA3A252025-10-23

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Primary DI, Brand, Company table
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00844868052494T3® PROZimVie US Corp LLCNDP2026-05-28
00844868052500T3® PROZimVie US Corp LLCNDP2026-05-28
00844868052517T3® PROZimVie US Corp LLCNDP2026-05-28
00844868052524T3® PROZimVie US Corp LLCNDP2026-05-28
00844868052531T3® PROZimVie US Corp LLCNDP2026-05-28
00844868052548T3® ShortZimVie US Corp LLCNDP2026-05-28
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