← Back to catalogue

Forefoot Ii

FDA UDI

Class I (US FDA UDI)

by Newdeal Sas

Identity

Trade Name
FOREFOOT II FDA UDI
Generic Name
Cannulated surgical drill bit, single-use FDA UDI
Device Name
AO "2 in 1" cannulated drill dia. 2.2/3.0mm L.22mm FDA UDI
Model / Reference
159025SND FDA UDI
Description
AO "2 in 1" cannulated drill dia. 2.2/3.0mm L.22mm FDA UDI

Identifiers

Catalog Number
159025S FDA UDI
Primary DI / UDI-DI
10381780045380 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Category: Cannulated surgical drill bit, single-use

Forefoot Ii by Newdeal Sas — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill bit, single-use.

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
Newdeal Sas

Sources (1)

  • FDA UDI 9d51ba9b-de2c-4800-b8b6-9c40c7154d5b 37 fields · synced May 31, 2026