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Best

FDA UDI

Class I (US FDA UDI)

by Lacey Manufacturing Company Llc

Identity

Trade Name
BEST FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Device Name
Sheathed Surgical Knife FDA UDI
Model / Reference
1571-00 FDA UDI
Description
Sheathed Surgical Knife FDA UDI

Identifiers

Catalog Number
1571-00 FDA UDI
Primary DI / UDI-DI
00853508002003 FDA UDI
FDA Product Code
HTS FDA UDI
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Prescription Use

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Scalpel, single-use

Best by Lacey Manufacturing Company Llc — 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 9786d1d4-9fc7-41cd-a00c-f45c7ce034f4 35 fields · synced Jun 1, 2026