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Epimed

FDA UDI

Class II (US FDA UDI)

by Epimed International, Inc

Identity

Trade Name
Epimed FDA UDI
Generic Name
Surgical/procedural instrument transport cabinet FDA UDI
Device Name
PainBlocker™ Cart FDA UDI
Model / Reference
400-PBCRT FDA UDI
Description
PainBlocker™ Cart FDA UDI

Identifiers

Catalog Number
400-PBCRT FDA UDI
Primary DI / UDI-DI
00818788022714 FDA UDI
FDA Product Code
GXH FDA UDI
GMDN Term
Surgical/procedural instrument transport cabinet FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Surgical/procedural instrument transport cabinet

Epimed by Epimed International, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/procedural instrument transport cabinet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Epimed International, Inc

Sources (1)

  • FDA UDI d782578a-09cf-4e6b-9986-8412fff49b66 36 fields · synced Jun 6, 2026