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Reli

FDA UDI

Class II (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name
RELI FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Device Name
REDILENE Monofilament Polypropylene 6-0 YP-3 18", FDA UDI
Model / Reference
P8695-P FDA UDI
Description
REDILENE Monofilament Polypropylene 6-0 YP-3 18", FDA UDI

Identifiers

Catalog Number
P8695-P FDA UDI
Primary DI / UDI-DI
00386120007816 FDA UDI
FDA Product Code
GAW FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5010 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

Dimensions & Sizes

Size
Length — 18 Inch FDA UDI

Category: Polyolefin/fluoropolymer suture, monofilament

Reli by Myco Medical Supplies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bc0d3d54-d57b-4dfd-8e83-98b548fdcaf9 35 fields · synced Jun 8, 2026