← Back to catalogue

Ibs™

FDA UDI

Class I (US FDA UDI)

by In2bones

Identity

Trade Name
IBS™ FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Model / Reference
G01 00782 FDA UDI

Identifiers

Catalog Number
G01 00782 FDA UDI
Primary DI / UDI-DI
03760225712566 FDA UDI
FDA Product Code
GFG FDA UDI
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
Not 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

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

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

Manufacturer
In2bones

Sources (1)

  • FDA UDI 4a66b7a3-661d-41b2-a929-2f6b3253bc62 35 fields · synced May 31, 2026