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Implant-One

FDA UDI

Class I (US FDA UDI)

by Implant Logistics, Inc.

Identity

Trade Name
Implant-One FDA UDI
Generic Name
Cannulated surgical drill guiding pin FDA UDI
Device Name
Bone Profiler, Guide Pin Green FDA UDI
Model / Reference
1156-1500-33 FDA UDI
Description
Bone Profiler, Guide Pin Green FDA UDI

Identifiers

Primary DI / UDI-DI
D76211561500330 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Cannulated surgical drill guiding pin 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Cannulated surgical drill guiding pin

Implant-One by Implant Logistics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill guiding pin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ac61319-4ae0-4fe6-b602-8ab85b5fcaf7 34 fields · synced May 30, 2026