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Anchorage

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ANCHORAGE FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
Template For Universal Cross-Plate FDA UDI
Model / Reference
705182 FDA UDI
Description
Template For Universal Cross-Plate FDA UDI

Identifiers

Catalog Number
705182 FDA UDI
Primary DI / UDI-DI
07613327131185 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 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

No

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

Category: Surgical implant template, reusable

Anchorage by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 4844efc9-4d49-4f41-aa4f-798d142b29f9 34 fields · synced May 31, 2026