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Barbiturate Panel Dip

FDA UDI

Class II (US FDA UDI)

by Assure Tech. (hangzhou) Co., Ltd.

Identity

Trade Name
Barbiturate Panel Dip FDA UDI
Generic Name
Barbiturate IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
1.0 FDA UDI

Identifiers

Primary DI / UDI-DI
06952804801700 FDA UDI
510(k) Number
K151211 FDA UDI
FDA Product Code
DIS FDA UDI
GMDN Term
Barbiturate IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3150 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

Yes

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: Barbiturate IVD, kit, rapid ICT, clinical

Barbiturate Panel Dip by Assure Tech. (hangzhou) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Barbiturate IVD, kit, rapid ICT, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22bf2efc-bde7-42e2-95c0-198d74588ba5 33 fields · synced Jun 8, 2026