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Salvin Dental Specialties

FDA UDI

Class I (US FDA UDI)

by Salvin Dental Specialties, Llc

Identity

Trade Name
Salvin Dental Specialties FDA UDI
Generic Name
General-purpose calliper, metallic FDA UDI
Device Name
3I Guide Narrow Platform FDA UDI
Model / Reference
IMPLANT-RESCUE-3I-NP FDA UDI
Description
3I Guide Narrow Platform FDA UDI

Identifiers

Catalog Number
IMPLANT-RESCUE-3I-NP FDA UDI
Primary DI / UDI-DI
00841336109575 FDA UDI
FDA Product Code
KTZ FDA UDI
GMDN Term
General-purpose calliper, metallic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4150 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose calliper, metallic

Salvin Dental Specialties by Salvin Dental Specialties, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose calliper, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2f0c9f9-1627-441f-b93e-f07b057c1501 34 fields · synced Jun 6, 2026