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Post Medical, Inc.

FDA UDI

Class II (US FDA UDI)

by Post Medical, Inc.

Identity

Trade Name
Post Medical, Inc. FDA UDI
Generic Name
Sharps container FDA UDI
Model / Reference
WD-200 FDA UDI

Identifiers

Catalog Number
WD-200 FDA UDI
Primary DI / UDI-DI
B309WD2000 FDA UDI
510(k) Number
K925816 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Sharps container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sharps container

Post Medical, Inc. by Post Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sharps container.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Post Medical, Inc.

Sources (1)

  • FDA UDI 500c2e86-bd46-4a4c-8e63-134a3b1e4b66 34 fields · synced May 30, 2026