← Back to catalogue

Exel Srgcl Blade, S-S, Size:12

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 29504

by Exelint International, Co.

Identity

Trade Name
EXEL SRGCL BLADE,S-S, SIZE:12 EUDAMEDFDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
EXEL SURGICAL BLADE EUDAMED
EXEL SRGCL BLADE,S-S, SIZE:12; 100/BX, 1000/CS, 10CS/CRTN FDA UDI
Model / Reference
29504 EUDAMEDFDA UDI
Description
EXEL SRGCL BLADE,S-S, SIZE:12; 100/BX, 1000/CS, 10CS/CRTN FDA UDI

Identifiers

Catalog Number
29504 FDA UDI
Primary DI / UDI-DI
00020221295047 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221295047 EUDAMED
FDA Product Code
GES FDA UDI
EMDN Code
V010302 BLADES WITHOUT SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Manual scalpel blade, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Exel Srgcl Blade, S-S, Size:12 by Exelint International, Co. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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

EUDAMED SRN
US-MF-000037396
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 6e368763-124c-4209-a736-a43637d75914 61 fields · synced Oct 5, 2026
  • FDA UDI cb275dc0-b9ea-4665-936f-c923feb2dd20 35 fields · synced May 30, 2026