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Micro-Blade (K) 31-1002

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 31-1002

by Charmant Inc.

Identity

Trade Name
Micro-Blade(K) FDA UDI
Generic Name
Dura mater knife FDA UDI
Device Name
Micro-Blade (K) 31-1002 EUDAMED
Model / Reference
31-1002 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00883475950953 EUDAMEDFDA UDI
Basic UDI-DI
B-00883475950953 EUDAMED
FDA Product Code
EMF FDA UDI
EMDN Code
L0102 SURGICAL KNIVES, REUSABLE EUDAMED
GMDN Term
Dura mater knife FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Micro-Blade (K) 31-1002 by Charmant Inc. — Class I — 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

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Manufacturer

Manufacturer
Charmant Inc.
EUDAMED SRN
JP-MF-000023565
Authorised Representative
Charmant GmbH Europe DE-AR-000022071

Sources (2)

  • EUDAMED c083acd3-4a46-4a8b-8f21-a3224a4f7fbf 61 fields · synced Jun 17, 2026
  • FDA UDI 07b03943-17bd-4ec8-9122-ad68b7dbd6d8 32 fields · synced May 29, 2026