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Graftmaster

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
GRAFTMASTER FDA UDI
Generic Name
Tendon/ligament graft preparation station base FDA UDI
Device Name
GRAFTMASTER III TISSUE GRASPER 2 FDA UDI
Model / Reference
72202315 FDA UDI
Description
GRAFTMASTER III TISSUE GRASPER 2 FDA UDI

Identifiers

Catalog Number
72202315 FDA UDI
Primary DI / UDI-DI
03596010651112 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Tendon/ligament graft preparation station base FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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: Tendon/ligament graft preparation station base

Graftmaster by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament graft preparation station base.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 4b46c103-e60c-4180-bc7e-a9206ca89d70 35 fields · synced Jun 8, 2026