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Rospital Productos Medicos

FDA UDI

Class I (US FDA UDI)

by Atlas Medical Products Llc

Identity

Trade Name
Rospital Productos Medicos FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
SURGICAL BLADES W/PLASTIC HANDLE #12 EA. FDA UDI
Model / Reference
SBP12 FDA UDI
Description
SURGICAL BLADES W/PLASTIC HANDLE #12 EA. FDA UDI

Identifiers

Catalog Number
SBP12 FDA UDI
Primary DI / UDI-DI
00812460028025 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Manual scalpel blade, 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

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: Manual scalpel blade, single-use

Rospital Productos Medicos by Atlas Medical Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 780867ba-ddb4-4e80-b30b-e16510e74f63 36 fields · synced Jun 6, 2026