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Life Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 811-1105-1

by Life Instrument Corporation

Identity

Trade Name
Curette EUDAMED
Life Instruments FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
Curettes / Rasps EUDAMED
Cobb Curette #5 Ang FDA UDI
Model / Reference
811-1105-1 EUDAMEDFDA UDI
Description
Cobb Curette #5 Ang FDA UDI

Identifiers

Primary DI / UDI-DI
M930811110510 EUDAMEDFDA UDI
Basic UDI-DI
++M930001PT EUDAMED
FDA Product Code
FZS FDA UDI
EMDN Code
L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE EUDAMED
GMDN Term
Bone curette, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Spain 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

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

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

No

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

Life Instruments by Life Instrument Corporation — Class I — FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 8867085d-7fe1-4c50-811e-6def44374b72 33 fields · synced Oct 6, 2026
  • EUDAMED d8d23e45-8855-4f94-a9f2-7522fd60d3b6 61 fields · synced Jul 29, 2026