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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
Polyglycolic acid suture FDA UDI
Device Name
REDISORB Undyed Braided & Coated Polyglycolic Acid, 5-0, MPS-2 FDA UDI
Model / Reference
VU495-SI FDA UDI
Description
REDISORB Undyed Braided & Coated Polyglycolic Acid, 5-0, MPS-2 FDA UDI

Identifiers

Primary DI / UDI-DI
00386120006178 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyglycolic acid suture 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

No

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 — 27 Inch FDA UDI

Category: Polyglycolic acid suture

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

Similar devices

Also classified as Polyglycolic acid suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b7c35749-4d68-4b54-b62e-3e7a27d8b905 34 fields · synced May 30, 2026