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Truepill Inc.

FDA UDI

Class I (US FDA UDI)

by Postmeds, Inc.

Identity

Trade Name
Truepill Inc. FDA UDI
Generic Name
Specimen container mailer, non-insulated FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
00850032976114 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
Specimen container mailer, non-insulated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen container mailer, non-insulatedSpecimen stabilization reagent IVD

Truepill Inc. by Postmeds, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen stabilization reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Postmeds, Inc.

Sources (1)

  • FDA UDI cdc99f1e-4dc1-457c-b1e8-73c609e12091 32 fields · synced Jun 8, 2026