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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
Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
Device Name
REDISORB PRO VIO BR 0 YCT-1 30" FDA UDI
Model / Reference
V340-M FDA UDI
Description
REDISORB PRO VIO BR 0 YCT-1 30" FDA UDI

Identifiers

Catalog Number
V340-M FDA UDI
Primary DI / UDI-DI
00386120010144 FDA UDI
510(k) Number
K172659 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 30 Inch FDA UDI

Category: Polyester suture, bioabsorbable, multifilament, non-antimicrobial

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

Similar devices

Also classified as Polyester suture, bioabsorbable, multifilament, non-antimicrobial.

Cleared under the same submission

K172659 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Myco Medical Supplies Inc.

Sources (1)

  • FDA UDI b46ea804-0f77-448c-8a23-7252f48f20d7 37 fields · synced May 31, 2026