← Back to catalogue

Ram® Cor-Suture®, 2-0 Pe White

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 022320

by LSI SOLUTIONS, Inc.

Identity

Trade Name
RAM® COR-SUTURE®, 2-0 PE WHITE EUDAMED
RAM® COR-SUTURE® QUICK LOAD® FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
RAM® COR-SUTURE®, 2-0 PE WHITE EUDAMED
RAM® COR-SUTURE® QUICK LOAD® SINGLES 3.5MM, NON-PLEDGETED, 2-0 POLYESTER, WHITE, NON-ABSORBABLE, 38" FDA UDI
Model / Reference
022320 EUDAMEDFDA UDI
Description
RAM® COR-SUTURE® QUICK LOAD® SINGLES 3.5MM, NON-PLEDGETED, 2-0 POLYESTER, WHITE, NON-ABSORBABLE, 38" FDA UDI

Identifiers

Catalog Number
022320 FDA UDI
Primary DI / UDI-DI
00850200006469 EUDAMEDFDA UDI
Basic UDI-DI
B-00850200006469 EUDAMED
510(k) Number
K160529 FDA UDI
K203081 FDA UDI
FDA Product Code
GAS FDA UDI
EMDN Code
H0102010299 SYNTHETIC NONABSORBABLE MULTIFILAMENT SUTURES - OTHER EUDAMED
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 — 38 Inch FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

Ram® Cor-Suture®, 2-0 Pe White by LSI Solutions, Inc. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
LSI SOLUTIONS, Inc.
EUDAMED SRN
US-MF-000008267
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 6f6508e5-2fdc-44d4-b9af-e8c76589bede 61 fields · synced Jun 17, 2026
  • FDA UDI f0f90a87-e1bb-4683-9989-410a6a44c868 37 fields · synced May 29, 2026