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HNM Medical

FDA UDI

Class I (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name
HNM Medical FDA UDI
Generic Name
Rectal speculum FDA UDI
Device Name
SIMS RECTAL SPECULUM, 6 1/4", 1/2"X3" FENESTRATED BLADES FDA UDI
Model / Reference
HNM-1-50-7305 FDA UDI
Description
SIMS RECTAL SPECULUM, 6 1/4", 1/2"X3" FENESTRATED BLADES FDA UDI

Identifiers

Catalog Number
HNM-1-50-7305 FDA UDI
Primary DI / UDI-DI
00842962123751 FDA UDI
FDA Product Code
FFQ FDA UDI
GMDN Term
Rectal speculum FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rectal speculum

HNM Medical by Hnm Stainless, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rectal speculum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hnm Stainless, Llc.

Sources (1)

  • FDA UDI 6daa658f-afde-4727-9ca4-214c78971b6b 34 fields · synced May 30, 2026