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Hdc

FDA UDI

by Hdc Corp.

Identity

Trade Name
HDC FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
ORGANIZER FOR SPIDER PIN FDA UDI
Model / Reference
CSS-3006 FDA UDI
Description
ORGANIZER FOR SPIDER PIN FDA UDI

Identifiers

Catalog Number
CSS-3006 FDA UDI
Primary DI / UDI-DI
08057013140041 FDA UDI
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

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

Hdc by Hdc Corp. — 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

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Manufacturer

Manufacturer
Hdc Corp.

Sources (1)

  • FDA UDI f7df9c59-f3ae-4c4e-9ec6-df91ec441753 34 fields · synced May 30, 2026