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J&J Instruments

FDA UDI

Class I (US FDA UDI)

by J&J Instruments, LLC

Identity

Trade Name
J&J Instruments FDA UDI
Generic Name
Dental rongeur FDA UDI
Device Name
BLUMENTHAL RONGEUR 6"" 45d FDA UDI
Model / Reference
11-045 FDA UDI
Description
BLUMENTHAL RONGEUR 6"" 45d FDA UDI

Identifiers

Primary DI / UDI-DI
00817524024135 FDA UDI
FDA Product Code
EKD FDA UDI
GMDN Term
Dental rongeur 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

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 rongeur

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

Similar devices

Also classified as Dental rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bba7f2a8-a9b4-4dcf-98ca-519c75a94c70 33 fields · synced Jun 9, 2026