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Senhance USB-C LIA Drape

EUDAMEDFDA UDI

Class I (EU MDR)

Ref X9007763 Senhance USB-C LIA CableModel X9007763

by DAS Medical International, SRL

Identity

Trade Name
Senhance USB-C LIA Drape EUDAMED
Asensus FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Senhance USB-C LIA Cable EUDAMED
Senhance USB-C LIA Drape EUDAMED
Senhance USB-C LIA Drape (X9007763) FDA UDI
Model / Reference
X9007763 EUDAMEDFDA UDI
X9007763 Senhance USB-C LIA Cable EUDAMED
Description
Senhance USB-C LIA Drape (X9007763) FDA UDI

Identifiers

Catalog Number
X9007763 FDA UDI
Primary DI / UDI-DI
07466532979246 EUDAMEDFDA UDI
27466532979240 EUDAMED
Basic UDI-DI
B-07466532979246 EUDAMED
746742323X90077638W EUDAMED
Direct Marketing DI
27466532979240 EUDAMED
FDA Product Code
PUI FDA UDI
EMDN Code
T020199 SURGICAL DRAPES - OTHER EUDAMED
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Market of Registration
Bulgaria 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
Sterilization Method
Ethylene Oxide FDA UDI

Senhance USB-C LIA Drape by Das Medical International, Srl — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
DO-MF-000034519
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (3)

  • EUDAMED c8ac3a1d-b110-423d-a631-eb07073f991c 61 fields · synced Jul 21, 2026
  • FDA UDI 0db58d80-1e3a-404d-a397-c1ff244fa6ca 35 fields · synced May 30, 2026
  • EUDAMED 4781b64a-e3ad-42dc-8922-8ca24298ad86 61 fields · synced Jun 18, 2026