← Back to catalogue

Supplementary Drills Set

FDA UDI

Class I (US FDA UDI)

by Sweden & Martina Inc

Identity

Trade Name
SUPPLEMENTARY DRILLS SET FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
SUPPLEMENTARY DRILLS SET PRAMA DRILLS SHN GS 5.0 SUPPLEMENTARY DRILLS SET PRAMA DRILLS GS 5.0 FDA UDI
Model / Reference
GS-50-L-FSHN-INTEGRA FDA UDI
Description
SUPPLEMENTARY DRILLS SET PRAMA DRILLS SHN GS 5.0 SUPPLEMENTARY DRILLS SET PRAMA DRILLS GS 5.0 FDA UDI

Identifiers

Catalog Number
GS-50-L-FSHN-INTEGRA FDA UDI
Primary DI / UDI-DI
D7702694253 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Supplementary Drills Set by Sweden & Martina Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, 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 c78d393e-297f-4737-87d9-ca2daceed181 35 fields · synced May 30, 2026