Identity

Trade Name
Cadwell FDA UDI
Generic Name
Polysomnograph FDA UDI
Device Name
Piezo Buckle Kit SNAP Labs FDA UDI
Model / Reference
302529-200-0000 FDA UDI
Description
Piezo Buckle Kit SNAP Labs FDA UDI

Identifiers

Primary DI / UDI-DI
00840067103807 FDA UDI
510(k) Number
K903300 FDA UDI
GMDN Term
Polysomnograph FDA UDI

Classification

Commercial Distribution
Not 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Cadwell by Cadwell Industries, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7c736c52-26a7-4515-aec6-4336e94c73cf 36 fields · synced Jun 9, 2026