← Back to catalogue

Thermoplastic

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Thermoplastic FDA UDI
Generic Name
Patient positioning thermoplastic mould material FDA UDI
Device Name
Disposable non-sterile (39.4 x 55.9cm) solid perforated thermoplastic (3.2mm) FDA UDI
Model / Reference
MTBBA1522S FDA UDI
Description
Disposable non-sterile (39.4 x 55.9cm) solid perforated thermoplastic (3.2mm) FDA UDI

Identifiers

Catalog Number
MTBBA1522S FDA UDI
Primary DI / UDI-DI
00841439103906 FDA UDI
510(k) Number
K080072 FDA UDI
K093738 FDA UDI
K933227 FDA UDI
FDA Product Code
LNH FDA UDI
IYE FDA UDI
GMDN Term
Patient positioning thermoplastic mould material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1000 FDA UDI
892.5050 FDA UDI
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

No

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 22 Inch FDA UDI

Thermoplastic by Medtec LLC — Class II — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI 392c023e-ff63-47fb-b6a8-7555f33ed5e6 39 fields · synced Jun 6, 2026