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Sterile Surgical gloves 7521F

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 6410FModel 7521, 7529, 7621, 7629, 7521F, 7529F, 7621S, 7629S

by Motex Healthcare (anhui) Co., Ltd.

Identity

Trade Name
Sterile Surgical gloves 7521F EUDAMED
MocareHealth FDA UDI
Generic Name
Hevea-latex surgical glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Sterile Surgical gloves EUDAMED
Sterile Polyisoprene Powder-Free Surgical Gloves - Blue FDA UDI
Model / Reference
7521, 7529, 7621, 7629, 7521F, 7529F, 7621S, 7629S EUDAMED
6410F EUDAMED
7521F/7 FDA UDI
Description
Sterile Polyisoprene Powder-Free Surgical Gloves - Blue FDA UDI

Identifiers

Primary DI / UDI-DI
26971384153683 EUDAMEDFDA UDI
Basic UDI-DI
697138415CPI20004NF EUDAMED
510(k) Number
K063757 FDA UDI
FDA Product Code
KGO FDA UDI
EMDN Code
T01010203 POLYISOPREN SURGICAL GLOVES EUDAMED
GMDN Term
Hevea-latex surgical glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4460 FDA UDI
Market of Registration
Germany 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Sterile Surgical gloves 7521F by Motex Healthcare (anhui) Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CN-MF-000014097
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (2)

  • EUDAMED 6815da95-a7db-4f28-b399-e50831189b8f 61 fields · synced Jul 9, 2026
  • FDA UDI c247628d-6183-4bc0-8888-986216cdb980 34 fields · synced May 30, 2026