Duns Number:118270502
Device Description: P4: Package of four GHB premium handles. A “P” handle (Premium-Lock handle) consists of a P4: Package of four GHB premium handles. A “P” handle (Premium-Lock handle) consists of a standard, round, threaded, aluminum handle which embodies a micro-chuck assembly (MCA) and perforated pin-locking handle. A MCA embodies a threaded end which screws into the handle’s internal threads in order to secure a dental cutting bur so it cannot dislodge. To secure a dental bur after insertion, a bur-locking-wrench grips the MCA and is counter-tightened by a stainless steel locking pin at the handle’s opposite end. The “P” model MCA is ideal for users who like the flexibility of chair-side bur changing when desired, but multi-handle operation for maximum efficiency otherwise. The MCA’s outer sleeve embodies two locking grooves or slots that engage a 7 mm bur-locking “wrench” or “key.” It is made of durable, 2 mm thick, 6061-T6 medical grade aluminum. Designed for maximum strength and longevity, the MCA can withstand the demands of repeated bur-tightening common to a busy dental practice engaged in chair-side bur changing. This is why this model is classed as a “premium” model. Finally, both aluminum components, handle and MCA, are shielded from excessive friction and wear from routine tightening, by a durable, anti-friction stainless steel washer. The “P4” pack includes operational accessories. Learn more about our mission at dentalcareforall.org. If anyone has any complaints with our hand-burs, we ask that they please email or call us at team@dcfai.org or +19562801708 (same as Whatsapp number) so we can make it right, whatever we have to do.
Catalog Number
-
Brand Name
Gentle Hand-Bur Systems
Version/Model Number
P4
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
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For Single-Use
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Prescription Use (Rx)
-
Over the Counter (OTC)
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Kit
-
Combination Product
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Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DZN
Product Code Name
Instruments, Dental Hand
Public Device Record Key
73096309-0cdf-4883-8b9b-5cd6db47c1c7
Public Version Date
June 13, 2022
Public Version Number
1
DI Record Publish Date
June 05, 2022
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 5 |