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Gm

FDA UDI

Class I (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
GM FDA UDI
Generic Name
Intrauterine cannula, reusable FDA UDI
Device Name
6MM UTERINE SUCTION TIP FDA UDI
Model / Reference
01-90-8820 FDA UDI
Description
6MM UTERINE SUCTION TIP FDA UDI

Identifiers

Primary DI / UDI-DI
00026072025048 FDA UDI
FDA Product Code
HCY FDA UDI
GMDN Term
Intrauterine cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intrauterine cannula, reusable

Gm by Allied Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intrauterine cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI ffb58297-0b57-4570-8161-702536bd8629 33 fields · synced Jun 1, 2026