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OsteoMed

FDA UDI

Class II (US FDA UDI)

by Osteomed Corp.

Identity

Trade Name
OsteoMed FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
2.8mm x 230mm Threaded Guide Wire, Sterile, 2 Pk FDA UDI
Model / Reference
316-1702-SP-02 FDA UDI
Description
2.8mm x 230mm Threaded Guide Wire, Sterile, 2 Pk FDA UDI

Identifiers

Catalog Number
316-1702-SP-02 FDA UDI
Primary DI / UDI-DI
00842528110003 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.8 Millimeter FDA UDI

Category: Surgical drill guide, reusable

OsteoMed by Osteomed Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osteomed Corp.

Sources (1)

  • FDA UDI 3a84f0a4-a616-482d-8641-94e1e9e0362a 37 fields · synced Jun 6, 2026