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everpure

FDA UDI

Class I (US FDA UDI)

by Shanghai Everpure Plastics Co., Ltd.

Identity

Trade Name
everpure FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Model / Reference
DYND36600 FDA UDI

Identifiers

Primary DI / UDI-DI
06975803581237 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
General specimen container IVD, no additive/medium 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen container IVD, no additive/medium

everpure by Shanghai Everpure Plastics Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shanghai Everpure Plastics Co., Ltd.

Sources (1)

  • FDA UDI 3a9a4711-2b37-4dc1-8851-32b4bb069027 32 fields · synced May 30, 2026