Identity

Trade Name
MSP FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Device Name
3.5 MM RS ANG BU HDL 6PK FDA UDI
Model / Reference
56B350RDK FDA UDI
Description
3.5 MM RS ANG BU HDL 6PK FDA UDI

Identifiers

Primary DI / UDI-DI
00848782027071 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

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

Category: Scalpel, single-use

Msp by Surgical Specialties México, S. de R.L. de C.V. — 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 23eb591a-ce3f-49fa-8fdf-6c2506a7cb21 35 fields · synced May 30, 2026