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Bishop Bone Clamp

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BISHOP BONE CLAMP FDA UDI
Generic Name
Bone approximation clamp FDA UDI
Device Name
BISHOP BONE CLAMP WITH RATCHET FDA UDI
Model / Reference
305-380 FDA UDI
Description
BISHOP BONE CLAMP WITH RATCHET FDA UDI

Identifiers

Catalog Number
305-380 FDA UDI
Primary DI / UDI-DI
00192896027077 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 — 12.5 Inch FDA UDI

Category: Bone approximation clamp

Bishop Bone 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

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Manufacturer

Sources (1)

  • FDA UDI 13e213c8-3071-45f5-8258-6b04bed60b10 36 fields · synced Jun 1, 2026