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Carate

FDA UDI

Class II (US FDA UDI)

by Tianchang Jiarui Medical Material Co., Ltd.

Identity

Trade Name
CARATE FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
self sealing pouch SPH2338 57*100mm FDA UDI
Model / Reference
sterilization pouch FDA UDI
Description
self sealing pouch SPH2338 57*100mm FDA UDI

Identifiers

Primary DI / UDI-DI
06976310510086 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sterilization packaging, single-use

Carate by Tianchang Jiarui Medical Material Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f340b3c7-e1ce-47c4-b1c5-6e28962f9f7c 33 fields · synced May 30, 2026