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Sage

FDA UDI

Class I (US FDA UDI)

by Sage Products Llc

Identity

Trade Name
Sage FDA UDI
Generic Name
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
Sage AirTAP LC FDA UDI
Model / Reference
700-115 FDA UDI
Description
Sage AirTAP LC FDA UDI

Identifiers

Catalog Number
700-115 FDA UDI
Primary DI / UDI-DI
00618029980045 FDA UDI
FDA Product Code
FMP FDA UDI
KME FDA UDI
FSA FDA UDI
FMR FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
880.6060 FDA UDI
880.5510 FDA UDI
880.6785 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 65.0 Inch FDA UDI
Width — 37.0 Inch FDA UDI

Sage by Sage Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sage Products Llc

Sources (1)

  • FDA UDI 01772b08-a6f9-4b69-bbb9-aa8d9d9f470e 37 fields · synced Jun 8, 2026