← Back to catalogue

Microfix Quickanchor Orthocord

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
MICROFIX QUICKANCHOR ORTHOCORD FDA UDI
Generic Name
Tendon/ligament bone anchor, bioabsorbable FDA UDI
Device Name
MICROFIX QUICKANCHOR Plus (4/0 Suture) Poly (L-Lactide) Absorbable Anchor, Size 4/0 (1.5 metric) ORTHOCORD braided composite suture, 18 Inches (45cm) with J-1 reverse cutting needles and a 1.3 x 5.0mm drill bit FDA UDI
Model / Reference
212044 FDA UDI
Description
MICROFIX QUICKANCHOR Plus (4/0 Suture) Poly (L-Lactide) Absorbable Anchor, Size 4/0 (1.5 metric) ORTHOCORD braided composite suture, 18 Inches (45cm) with J-1 reverse cutting needles and a 1.3 x 5.0mm drill bit FDA UDI

Identifiers

Catalog Number
212044 FDA UDI
Primary DI / UDI-DI
10886705001897 FDA UDI
510(k) Number
K032078 FDA UDI
K080352 FDA UDI
K150209 FDA UDI
FDA Product Code
JDR FDA UDI
MAI FDA UDI
HWC FDA UDI
HTY FDA UDI
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, bioabsorbable 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

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

Category: Tendon/ligament bone anchor, bioabsorbable

Microfix Quickanchor Orthocord by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e87b7539-7826-4286-be80-d1a694322975 37 fields · synced May 30, 2026