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Cmc Med Solutions

FDA UDI

Class I (US FDA UDI)

by CMC Manufacturing Limited Liability Company

Identity

Trade Name
CMC MED SOLUTIONS FDA UDI
Generic Name
Body aspiration needle, single-use FDA UDI
Device Name
14G DECOMPRESSION NEEDLE 3.25 Inch FDA UDI
Model / Reference
14G-3.25 FDA UDI
Description
14G DECOMPRESSION NEEDLE 3.25 Inch FDA UDI

Identifiers

Primary DI / UDI-DI
00850067056003 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Body aspiration needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Body aspiration needle, single-use

Cmc Med Solutions by CMC Manufacturing Limited Liability Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body aspiration needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9df8b579-9cf5-45bb-8bb4-a2d27cbe0f40 35 fields · synced May 30, 2026