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Mediflex

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref SHM-S2P / 4107F-2

by Endosys Healthcare India Private Limited

Identity

Trade Name
SureStay EUDAMED
Mediflex FDA UDI
Generic Name
Surgical retractor/retraction system blade, single-use FDA UDI
Device Name
Surgical Stays - Skin Hooks EUDAMED
SureStay Elastic Beaded Stays 7mm Two Finger Sharp Hook 2 per pack / Skin Hooks, Sharp 2-fingers Moulded 2 per pack FDA UDI
Model / Reference
SHM-S2P / 4107F-2 EUDAMED
4107F-2 FDA UDI
Description
SureStay Elastic Beaded Stays 7mm Two Finger Sharp Hook 2 per pack / Skin Hooks, Sharp 2-fingers Moulded 2 per pack FDA UDI

Identifiers

Primary DI / UDI-DI
08904332600612 EUDAMEDFDA UDI
Basic UDI-DI
089043326SHS0038L EUDAMED
Unit of Use DI
08904332600568 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
Z12019099 VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - OTHER EUDAMED
GMDN Term
Surgical retractor/retraction system blade, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical retractor/retraction system blade, single-use

Mediflex by Endosys Healthcare India Private Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI c744e660-1ad8-4c4b-9ada-344a49d9ff17 33 fields · synced Jul 9, 2026
  • EUDAMED f19f3bd0-4365-43f0-b3a3-5230dee60cc4 61 fields · synced Jul 9, 2026