← Back to catalogue

Micro Bone Reduction Clamp

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Micro Bone Reduction Clamp FDA UDI
Generic Name
Bone approximation clamp FDA UDI
Device Name
Micro Bone Reduction Clamp With Sharp Ball Points and Hinge Ratchet FDA UDI
Model / Reference
1103-037CB FDA UDI
Description
Micro Bone Reduction Clamp With Sharp Ball Points and Hinge Ratchet FDA UDI

Identifiers

Catalog Number
1103-037CB FDA UDI
Primary DI / UDI-DI
00192896115279 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Bone approximation clamp 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 — 6.125 Inch FDA UDI

Category: Bone approximation clamp

Micro Bone Reduction Clamp by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone approximation clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 99519a7c-e5f9-4c41-b2e1-2163b589794f 36 fields · synced May 30, 2026