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Feather Disposable Scalpel

FDA UDI

Class I (US FDA UDI)

by Feather Safety Razor Co., Ltd.

Identity

Trade Name
FEATHER DISPOSABLE SCALPEL FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Model / Reference
No.10 FDA UDI

Identifiers

Primary DI / UDI-DI
04902470026022 FDA UDI
FDA Product Code
GDX FDA UDI
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scalpel, single-use

Feather Disposable Scalpel by Feather Safety Razor Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 351bbe5b-921c-4f77-8d74-63986d1070ff 32 fields · synced Jun 8, 2026