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Ibs™

FDA UDI

Class I (US FDA UDI)

by In2bones

Identity

Trade Name
IBS™ FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
MODULAR HANDLE SMALL SIZE FDA UDI
Model / Reference
G01 00881 FDA UDI
Description
MODULAR HANDLE SMALL SIZE FDA UDI

Identifiers

Catalog Number
G01 00881 FDA UDI
Primary DI / UDI-DI
03760225710944 FDA UDI
FDA Product Code
GDZ FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument handle, non-torque-limiting

Ibs™ by In2bones — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
In2bones

Sources (1)

  • FDA UDI da74099c-73f8-46f2-85a7-7ecaa6e8616b 35 fields · synced Jun 6, 2026