← Back to catalogue

Delta

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
Delta FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
Twist drill hex end FDA UDI
Model / Reference
70-92806 FDA UDI
Description
Twist drill hex end FDA UDI

Identifiers

Catalog Number
70-92806 FDA UDI
Primary DI / UDI-DI
07613327594935 FDA UDI
510(k) Number
K070876 FDA UDI
FDA Product Code
HBE FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

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

Dimensions & Sizes

Size
Length — 50.0 Millimeter FDA UDI

Category: Fluted surgical drill bit, single-use

Delta by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

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
Stryker Leibinger

Sources (1)

  • FDA UDI 08cecd63-f23b-4806-aa2f-a20cbaba7f08 36 fields · synced May 30, 2026