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Long Driver For Global Impl.

FDA UDI

Class I (US FDA UDI)

by Sweden & Martina Inc

Identity

Trade Name
LONG DRIVER FOR GLOBAL IMPL. FDA UDI
Generic Name
Dental implant/prosthesis surgical procedure kit FDA UDI
Device Name
LONG DRIVER FOR GLOBAL IMPL. NON RETENTIVE FDA UDI
Model / Reference
U-BLP-OT275 FDA UDI
Description
LONG DRIVER FOR GLOBAL IMPL. NON RETENTIVE FDA UDI

Identifiers

Catalog Number
U-BLP-OT275 FDA UDI
Primary DI / UDI-DI
D7701021113 FDA UDI
FDA Product Code
NDP 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
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

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 implant/prosthesis surgical procedure kit

Long Driver For Global Impl. 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

Sources (1)

  • FDA UDI 643a5318-4c9f-4ba2-859a-d5626ea9a0f2 35 fields · synced May 31, 2026