← Back to catalogue

Fracture Repair Suture Kit

FDA UDI

by Riverpoint Medical Llc

Identity

Trade Name
Fracture Repair Suture Kit FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Device Name
Fracture Repair Suture Kit (Suture Kit - KIT702 is convenience kit containing multiple HS Fiber sutures (K190817; K153307, K220765)). FDA UDI
Model / Reference
110046456 FDA UDI
Description
Fracture Repair Suture Kit (Suture Kit - KIT702 is convenience kit containing multiple HS Fiber sutures (K190817; K153307, K220765)). FDA UDI

Identifiers

Primary DI / UDI-DI
00840277401380 FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polyolefin/fluoropolymer suture, multifilament

Fracture Repair Suture Kit by Riverpoint Medical Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, multifilament.

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

Manufacturer
Riverpoint Medical Llc

Sources (1)

  • FDA UDI aebc06b1-666b-4cad-867f-22c5f4e94306 33 fields · synced May 31, 2026