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J&J Instruments

FDA UDI

Class II (US FDA UDI)

by J&J Instruments, LLC

Identity

Trade Name
J&J Instruments FDA UDI
Generic Name
Dental anaesthesia syringe, reusable FDA UDI
Device Name
ASPIRATING SYRINGE "CW" FDA UDI
Model / Reference
07-800 FDA UDI
Description
ASPIRATING SYRINGE "CW" FDA UDI

Identifiers

Catalog Number
07-800 FDA UDI
Primary DI / UDI-DI
00817524020007 FDA UDI
FDA Product Code
EJI FDA UDI
GMDN Term
Dental anaesthesia syringe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6770 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

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

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Dental anaesthesia syringe, reusable

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

Similar devices

Also classified as Dental anaesthesia syringe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 92b30e84-e62c-4190-aa24-7b6bf1f49bc3 35 fields · synced Jun 9, 2026