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Expanding Innovations

FDA UDI

Class I (US FDA UDI)

by Expanding Innovations, Inc.

Identity

Trade Name
Expanding Innovations FDA UDI
Generic Name
Bone file/rasp, manual, reusable FDA UDI
Device Name
Bayonet Rasp, Straight FDA UDI
Model / Reference
EI3857 FDA UDI
Description
Bayonet Rasp, Straight FDA UDI

Identifiers

Primary DI / UDI-DI
00810166520096 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
Bone file/rasp, manual, reusable 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusable

Expanding Innovations by Expanding Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone file/rasp, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bcf477ba-5fe3-4aa0-8e15-796d960e4a52 34 fields · synced Jun 6, 2026