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Bone Holding Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BONE HOLDING FORCEPS FDA UDI
Generic Name
Bone cutter FDA UDI
Device Name
BONE HOLDING FORCEPS WITH RATCHET/K-WIRE GUIDE CURVED TIP FDA UDI
Model / Reference
1103-088 FDA UDI
Description
BONE HOLDING FORCEPS WITH RATCHET/K-WIRE GUIDE CURVED TIP FDA UDI

Identifiers

Catalog Number
1103-088 FDA UDI
Primary DI / UDI-DI
00192896051355 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bone cutter 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 — 6.75 Inch FDA UDI

Category: Bone cutter

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 cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abdd6b9a-3161-4a83-9ac0-811e5c2ea8a1 36 fields · synced May 29, 2026