← Back to catalogue

Guide Twist Drill

FDA UDI

Class I (US FDA UDI)

by SNUCONE Co., LTD.

Identity

Trade Name
GUIDE TWIST DRILL FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Model / Reference
GTD-3810 FDA UDI

Identifiers

Primary DI / UDI-DI
08800020849243 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Fixture/appliance dental drill bit, reusable

Guide Twist Drill by SNUCONE Co., LTD. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixture/appliance dental drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
SNUCONE Co., LTD.

Sources (1)

  • FDA UDI dac68f40-b4f2-45bc-86b9-5b114c6b048c 33 fields · synced Jun 6, 2026