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Rapidloc Ethibond

FDA UDI

Class II (US FDA UDI)

by DePuy Mitek, Inc.

Identity

Trade Name
RAPIDLOC ETHIBOND FDA UDI
Generic Name
Tendon/ligament bone anchor, bioabsorbable FDA UDI
Device Name
RAPIDLOC MENISCAL REPAIR-PLA TOPHAT / 12 Degrees Absorbable - PLA/PLA with Size 2/0 (3 metric) ETHIBOND Green braided polyester suture, and 12 Degrees curved needle FDA UDI
Model / Reference
228421 FDA UDI
Description
RAPIDLOC MENISCAL REPAIR-PLA TOPHAT / 12 Degrees Absorbable - PLA/PLA with Size 2/0 (3 metric) ETHIBOND Green braided polyester suture, and 12 Degrees curved needle FDA UDI

Identifiers

Catalog Number
228421 FDA UDI
Primary DI / UDI-DI
10886705010257 FDA UDI
510(k) Number
K002406 FDA UDI
FDA Product Code
GAM FDA UDI
MAI FDA UDI
GAS FDA UDI
GMDN Term
Tendon/ligament bone anchor, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 FDA UDI
888.3030 FDA UDI
878.5000 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Rapidloc Ethibond by DePuy Mitek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DePuy Mitek, Inc.

Sources (1)

  • FDA UDI 49955637-726b-4479-b722-0f62c6a85a21 38 fields · synced May 30, 2026