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Blade Handle (K) 31-1001S

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 31-1001S

by Charmant Inc.

Identity

Trade Name
Blade Handle Short FDA UDI
Generic Name
Dura mater knife FDA UDI
Device Name
Blade Handle (K) 31-1001S EUDAMED
Model / Reference
31-1001S EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00883475952612 EUDAMEDFDA UDI
Basic UDI-DI
B-00883475952612 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

Blade Handle (K) 31-1001S 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 290ebbc2-8932-4aa5-a885-d79911150469 61 fields · synced Jun 17, 2026
  • FDA UDI 6b8b9da4-76b6-4e69-8060-7a7418e8147e 32 fields · synced May 29, 2026