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Hand Driver For Titanium Cap

FDA UDI

Class I (US FDA UDI)

by Sweden & Martina Inc

Identity

Trade Name
HAND DRIVER FOR TITANIUM CAP FDA UDI
Generic Name
Dental implant/prosthesis surgical procedure kit FDA UDI
Device Name
HAND DRIVER FOR TITANIUM CAP FDA UDI
Model / Reference
AVV-CAP-TIT-1 FDA UDI
Description
HAND DRIVER FOR TITANIUM CAP FDA UDI

Identifiers

Catalog Number
AVV-CAP-TIT-1 FDA UDI
Primary DI / UDI-DI
D7700433513 FDA UDI
FDA Product Code
NDP FDA UDI
NHA FDA UDI
GMDN Term
Dental implant/prosthesis surgical procedure kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant/prosthesis surgical procedure kit

Hand Driver For Titanium Cap by Sweden & Martina Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant/prosthesis surgical procedure kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sweden & Martina Inc

Sources (1)

  • FDA UDI 5f6d11b2-4774-4278-a6e0-32cc73d298a8 35 fields · synced May 30, 2026