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J & J Instruments Inc

FDA UDI

Class I (US FDA UDI)

by J&J Instruments, LLC

Identity

Trade Name
J & J INSTRUMENTS INC FDA UDI
Generic Name
Periosteal elevator, reusable FDA UDI
Device Name
GOUGE ELEVATOR #34 FDA UDI
Model / Reference
04-334 FDA UDI
Description
GOUGE ELEVATOR #34 FDA UDI

Identifiers

Catalog Number
04-334 FDA UDI
Primary DI / UDI-DI
00817524021233 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Periosteal elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

Dimensions & Sizes

Size
Length — 5.875 Inch FDA UDI

Category: Periosteal elevator, reusable

J & J Instruments Inc by J&J Instruments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periosteal elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 985465ef-2861-447a-8013-fbd80782aa05 35 fields · synced Jun 9, 2026