Identity

Trade Name
Neodent FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
ZI TRANSMUCOSAL BONE TAP, D5.0X8 FDA UDI
Model / Reference
111.055 FDA UDI
Description
ZI TRANSMUCOSAL BONE TAP, D5.0X8 FDA UDI

Identifiers

Catalog Number
111.055 FDA UDI
Primary DI / UDI-DI
07899878065463 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Bone tap, 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 8 Millimeter FDA UDI
Outer Diameter — 5 Millimeter FDA UDI

Category: Bone tap, reusable

Neodent by JJGC Indústria e Comércio de Materiais Dentários S/A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, 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

Sources (1)

  • FDA UDI 97bf9923-665f-4dfd-8656-2363d7d1b781 37 fields · synced May 30, 2026