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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
Silk suture FDA UDI
Device Name
REDISILK PRO BLK BR 3-0 YFS-2 18" FDA UDI
Model / Reference
SK7772-M FDA UDI
Description
REDISILK PRO BLK BR 3-0 YFS-2 18" FDA UDI

Identifiers

Catalog Number
SK7772-M FDA UDI
Primary DI / UDI-DI
00386120010052 FDA UDI
510(k) Number
K172149 FDA UDI
FDA Product Code
GAP FDA UDI
GMDN Term
Silk suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5030 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 — 18 Inch FDA UDI

Category: Silk suture

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

Similar devices

Also classified as Silk suture.

Cleared under the same submission

K172149 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 a5cad369-433d-4f6f-a9f9-f2ce201b5683 37 fields · synced May 30, 2026