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Raleigh Bone Holding Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
RALEIGH BONE HOLDING FORCEPS FDA UDI
Generic Name
Bone holding forceps FDA UDI
Device Name
RALEIGH BONE HOLDING FORCEPS WITH SPEED LOCK FDA UDI
Model / Reference
1103-040C FDA UDI
Description
RALEIGH BONE HOLDING FORCEPS WITH SPEED LOCK FDA UDI

Identifiers

Catalog Number
1103-040C FDA UDI
Primary DI / UDI-DI
00192896050990 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bone holding forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Bone holding forceps

Raleigh Bone Holding Forceps by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c661a0ff-ba0c-492a-b651-3a8fac152489 36 fields · synced May 30, 2026