FIXIT & ecoFIX

FDA UDI

Class I (US FDA UDI)

by S.b.m

Identity

Trade Name: FIXIT & ecoFIX FDA UDI
Generic Name: Bone tap, reusable FDA UDI
Device Name: Punch Tap to be used with diameter 5.5 mm and 6.5 mm FIXIT and ecoFIX suture anchors for rotator cuff repair. FDA UDI
Model / Reference: Punch Tap - 5.5 mm and 6.5 mm FDA UDI
Description: Punch Tap to be used with diameter 5.5 mm and 6.5 mm FIXIT and ecoFIX suture anchors for rotator cuff repair. FDA UDI

Identifiers

Catalog Number: EPA9000241 FDA UDI
Primary DI / UDI-DI: 03760154009744 FDA UDI
FDA Product Code: HWX FDA UDI
GMDN Term: Bone tap, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone tap, reusable

FIXIT & ecoFIX by S.b.m — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: S.b.m

Sources (1)

FDA UDI 8d178862-4664-4565-aaf9-7ee755f801d6 34 fields · synced May 30, 2026