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Needle Adapter

FDA UDI

Class II (US FDA UDI)

by Dermatologic Lab And Supply, Inc.

Identity

Trade Name
Needle Adapter FDA UDI
Generic Name
Electrosurgical electrode extension FDA UDI
Device Name
ADAPTER, FOR DENTAL NEEDLE, 3/32in X 1 1/8in LONG SHAFT FDA UDI
Model / Reference
ADAPT/DNTL FDA UDI
Description
ADAPTER, FOR DENTAL NEEDLE, 3/32in X 1 1/8in LONG SHAFT FDA UDI

Identifiers

Catalog Number
ADAPT/DNTL FDA UDI
Primary DI / UDI-DI
00609960001272 FDA UDI
510(k) Number
K001029 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical electrode extension FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

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: Electrosurgical electrode extension

Needle Adapter by Dermatologic Lab And Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical electrode extension.

Cleared under the same submission

K001029 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dermatologic Lab And Supply, Inc.

Sources (1)

  • FDA UDI d4dda2f0-392f-4eef-95f0-3e861c981134 35 fields · synced Jun 1, 2026