ApeTape

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name: ApeTape FDA UDI
Generic Name: Polyolefin/fluoropolymer suture, multifilament FDA UDI
Device Name: White/Black UHMWPE Polyblend Non-Absorbable Suture Tape FDA UDI
Model / Reference: P64-30W-1440-12 FDA UDI
Description: White/Black UHMWPE Polyblend Non-Absorbable Suture Tape FDA UDI

Identifiers

Primary DI / UDI-DI: 00840277409850 FDA UDI
FDA Product Code: GAT FDA UDI
GMDN Term: Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.5000 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

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Polyolefin/fluoropolymer suture, multifilament

ApeTape by Riverpoint Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, multifilament.

Arthrex® — Arthrex, Inc. · Class II
FORCE FIBER — TELEFLEX INCORPORATED · Class II
Arthrex® — Arthrex, Inc. · Class II
HI-FI — TELEFLEX INCORPORATED · Class II
FORCE FIBER — TELEFLEX INCORPORATED · Class II
FORCE FIBER — TELEFLEX INCORPORATED · Class II
Arthrex® — Arthrex, Inc. · Class II
TELEFLEX — TELEFLEX INCORPORATED · Class II

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 II	Pending data

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

Manufacturer

Manufacturer: Riverpoint Medical Llc

Sources (1)

FDA UDI 3d72d38c-1779-4133-96c2-c750881b3e03 33 fields · synced May 31, 2026