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Foster & Thrive

FDA UDI

Class II (US FDA UDI)

by Mckesson Corp.

Identity

Trade Name
Foster & Thrive FDA UDI
Generic Name
Aneroid manual sphygmomanometer FDA UDI
Model / Reference
BPAG1-20MFT(2878106) FDA UDI

Identifiers

Primary DI / UDI-DI
00010939960184 FDA UDI
510(k) Number
K221857 FDA UDI
FDA Product Code
DXQ FDA UDI
LDE FDA UDI
GMDN Term
Aneroid manual sphygmomanometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 FDA UDI
870.1875 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Aneroid manual sphygmomanometer

Foster & Thrive by Mckesson Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aneroid manual sphygmomanometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Corp.

Sources (1)

  • FDA UDI 1f0b5ce0-3298-4d63-9680-abcc1139964f 33 fields · synced Jun 8, 2026