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Decker Micro Rongeur

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
DECKER MICRO RONGEUR FDA UDI
Generic Name
Craniofacial rongeur, reusable FDA UDI
Device Name
DECKER MICRO RONGEUR STRAIGHT TIP QUANTUM FDA UDI
Model / Reference
469-056Q FDA UDI
Description
DECKER MICRO RONGEUR STRAIGHT TIP QUANTUM FDA UDI

Identifiers

Catalog Number
469-056Q FDA UDI
Primary DI / UDI-DI
00192896093508 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Craniofacial rongeur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Craniofacial rongeur, reusable

Decker Micro Rongeur by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial rongeur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6755e8c8-32d4-456a-87d2-d4277717949e 36 fields · synced May 29, 2026