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Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
BELT SET, SOLID FETAL MONITOR TAB 1.5X36 FDA UDI
Model / Reference
1210BG2 FDA UDI
Description
BELT SET, SOLID FETAL MONITOR TAB 1.5X36 FDA UDI

Identifiers

Primary DI / UDI-DI
00840216119444 FDA UDI
FDA Product Code
ISR FDA UDI
GMDN Term
Personal device holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Personal device holder, reusable

Asp Medical by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Personal device holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 9eefd703-56eb-4ab9-97a4-7a4b1c52fc44 33 fields · synced Jun 1, 2026